Canonical Allele Identifier: PA2826634161
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142210
ClinVar RCV Id: RCV000131202

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Lys1050Gln
CA015349
NM_001281493.2:c.3148A>C