Canonical Allele Identifier: PA2825088168
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_000170.1:p.Glu463Lys
CA346745060
NM_000179.3:c.1387G>A