Canonical Allele Identifier: PA2826462797
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 231690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ser21Tyr
CA10577927
NM_001258281.1:c.62C>A