Canonical Allele Identifier: PA2499230004
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1037485
ClinVar RCV Id: RCV001340645 RCV002447397
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala771Thr
CA346729877
NM_000251.3:c.2311G>A