Canonical Allele Identifier: PA2826632324
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1403591
ClinVar RCV Id: RCV001898817

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Cys662Tyr
CA346756067
NM_001281493.2:c.1985G>A