Canonical Allele Identifier: PA2826628459
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 184794
ClinVar RCV Id: RCV000164110 RCV000506000 RCV000466573 RCV000589252 RCV000663282
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val1030Phe
CA013053
NM_001281492.2:c.3088G>T