Canonical Allele Identifier: PA2579921744
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1789628
ClinVar RCV Id: RCV002457592
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly775Asp
CA346729901
NM_000251.3:c.2324G>A