Canonical Allele Identifier: PA2580558720
Gene: FAM83H HGNC NCBI

Linked Data

ClinVar Variation Id: 2366705
ClinVar RCV Id: RCV002990539

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_940890.4:p.Arg378Trp
CA372468446
NM_198488.5:c.1132C>T