Canonical Allele Identifier: PA2826627974
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2743411
ClinVar RCV Id: RCV003593553

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg835Trp
CA346756077
NM_001281492.2:c.2503A>T