Canonical Allele Identifier: PA331416
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90823
ClinVar RCV Id: RCV000076325
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Pro652His
CA019605
NM_000251.3:c.1955C>A