Canonical Allele Identifier: PA2826625248
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2897463
ClinVar RCV Id: RCV003760283

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gln195Arg
CA346740975
NM_001281492.2:c.584A>G