Canonical Allele Identifier: PA915954657
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 821316
ClinVar RCV Id: RCV001015613 RCV001860800
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val821Ile
CA346730515
NM_000251.3:c.2461G>A