Canonical Allele Identifier: PA2573192901
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1412040
ClinVar RCV Id: RCV001923048
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Lys989Gln
CA346761355
NM_001281494.2:c.2965A>C