Canonical Allele Identifier: PA915966623
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 820584
ClinVar RCV Id: RCV001014184 RCV002551768
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly68Val
CA346729056
NM_000251.3:c.203G>T