Canonical Allele Identifier: PA2579922543
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2191723
ClinVar RCV Id: RCV002632964

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Cys822Ser
CA346730529
NM_000251.3:c.2464T>A
CA346730537
NM_000251.3:c.2465G>C