Canonical Allele Identifier: PA2826634685
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1510374
ClinVar RCV Id: RCV002011719
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser157Thr
CA346744938
NM_001281494.2:c.469T>A