Canonical Allele Identifier: PA2826465533
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 939657
ClinVar RCV Id: RCV001209085 RCV002451450
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn733Lys
CA035563
NM_001258281.1:c.2199T>A
CA346730180
NM_001258281.1:c.2199T>G