Canonical Allele Identifier: PA2825090004
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2453198
ClinVar RCV Id: RCV003182653
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu899Asp
CA346755312
NM_000179.3:c.2697A>C
CA346755313
NM_000179.3:c.2697A>T