Canonical Allele Identifier: PA658672976
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 483660
ClinVar RCV Id: RCV000561684 RCV000698314 RCV000758591 RCV001764664
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala765Val
CA346729845
NM_000251.3:c.2294C>T