Canonical Allele Identifier: PA2579910283
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1796436
ClinVar RCV Id: RCV002441810
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu94Pro
CA346729590
NM_000251.3:c.281T>C