Canonical Allele Identifier: PA645471150
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237361
ClinVar RCV Id: RCV000230826 RCV000575441 RCV003998753
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asp41Tyr
CA10581991
NM_000251.3:c.121G>T