Canonical Allele Identifier: PA2826625843
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2567486
ClinVar RCV Id: RCV003278528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly337Cys
CA346745160
NM_001281492.2:c.1009G>T