Canonical Allele Identifier: PA2826625092
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2587335
ClinVar RCV Id: RCV003360813

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly159Ser
CA346740611
NM_001281492.2:c.475G>A