Canonical Allele Identifier: PA2826628339
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455253

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val1002Leu
CA070770
NM_001281492.2:c.3004G>C