Canonical Allele Identifier: PA658738986
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 489929
ClinVar RCV Id: RCV000579590 RCV001240812 RCV001574074 RCV004001257
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr677Ala
CA346729112
NM_000251.3:c.2029A>G