Canonical Allele Identifier: PA2826625889
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 628958
ClinVar RCV Id: RCV000773625
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys349Thr
CA346745564
NM_001281492.2:c.1046A>C