Canonical Allele Identifier: PA2826634228
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1765963
ClinVar RCV Id: RCV002378792

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr3Ile
CA346740728
NM_001281494.2:c.8C>T