Canonical Allele Identifier: PA2826627103
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455185
ClinVar RCV Id: RCV000528774

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg631Met
CA346752899
NM_001281492.2:c.1892G>T