Canonical Allele Identifier: PA2826629555
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1332141
ClinVar RCV Id: RCV001804657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Lys15Thr
CA346740822
NM_001281493.2:c.44A>C