Canonical Allele Identifier: PA2826630485
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 960050
ClinVar RCV Id: RCV001233505

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Lys235Thr
CA346747012
NM_001281493.2:c.704A>C