Canonical Allele Identifier: PA2826464927
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2847396
ClinVar RCV Id: RCV003758534

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile585Phe
CA346728758
NM_001258281.1:c.1753A>T