Canonical Allele Identifier: PA2579913765
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3076128
ClinVar RCV Id: RCV004018445
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Tyr299His
CA346732930
NM_000251.3:c.895T>C