Canonical Allele Identifier: PA645475595
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 232707
ClinVar RCV Id: RCV000220420 RCV001053718
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly761Val
CA10578002
NM_000251.3:c.2282G>T