Canonical Allele Identifier: PA299355
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182578
ClinVar RCV Id: RCV000160609 RCV000218725 RCV000456427 RCV003453268
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala763Val
CA020406
NM_000251.3:c.2288C>T