Canonical Allele Identifier: PA2826465019
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90858
ClinVar RCV Id: RCV000759107 RCV003452880 RCV003758687 RCV004019108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn605Lys
CA019811
NM_001258281.1:c.1815T>A
CA346729085
NM_001258281.1:c.1815T>G