Canonical Allele Identifier: PA2579919049
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3072568
ClinVar RCV Id: RCV004013590
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly614Ala
CA346728399
NM_000251.3:c.1841G>C