Canonical Allele Identifier: PA299369
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182583
ClinVar RCV Id: RCV000233177 RCV000410808 RCV000565216 RCV000590509 RCV001251062 RCV002478486 RCV003483528 RCV003998484
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala189Gly
CA021433
NM_000251.3:c.566C>G