Canonical Allele Identifier: PA645471131
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 231095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Pro30Arg
CA10577916
NM_000251.3:c.89C>G