Canonical Allele Identifier: PA2826635623
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2808405
ClinVar RCV Id: RCV003760767

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Lys374Thr
CA346750713
NM_001281494.2:c.1121A>C