Canonical Allele Identifier: PA2826625176
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 855477
ClinVar RCV Id: RCV001060757 RCV003462585
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser179Pro
CA346740748
NM_001281492.2:c.535T>C