Canonical Allele Identifier: PA331209
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90507
ClinVar RCV Id: RCV000076002 RCV001213427
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu341Pro
CA016875
NM_000251.3:c.1022T>C