Canonical Allele Identifier: PA164955
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141266
ClinVar RCV Id: RCV000129706 RCV001065111 RCV003997517
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu357Asp
CA017034
NM_000251.3:c.1071G>C
CA346733271
NM_000251.3:c.1071G>T