Canonical Allele Identifier: PA2826464457
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182565
ClinVar RCV Id: RCV000160593 RCV000774571 RCV001067826 RCV003462090 RCV003998474
ClinVar Variation Id: 629230
ClinVar RCV Id: RCV000773929 RCV002290018 RCV004001338
ClinVar Variation Id: 1776525
ClinVar RCV Id: RCV002401003
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Phe473Leu
CA018746
NM_001258281.1:c.1419T>A
CA346727924
NM_001258281.1:c.1417T>C
CA346727929
NM_001258281.1:c.1419T>G