Canonical Allele Identifier: PA094635
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90789
ClinVar RCV Id: RCV000811456 RCV002399464
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala600Val
CA019334
NM_000251.3:c.1799C>T