Canonical Allele Identifier: PA2826625817
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2609841
ClinVar RCV Id: RCV003364334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly330Cys
CA346744970
NM_001281492.2:c.988G>T