Canonical Allele Identifier: PA174881
Gene: FAM83C HGNC NCBI

Linked Data

ClinVar Variation Id: 161837
ClinVar RCV Id: RCV000149373

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_848563.1:p.Arg288His
CA174880
NM_178468.6:c.863G>A