Canonical Allele Identifier: PA2826630176
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2162051
ClinVar RCV Id: RCV003078884
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu161Lys
CA346745060
NM_001281493.2:c.481G>A