Canonical Allele Identifier: PA2826627080
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1013697
ClinVar RCV Id: RCV001312322

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu625Lys
CA346752768
NM_001281492.2:c.1873G>A