Canonical Allele Identifier: PA2827349104
Gene: FAM114A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 92026
ClinVar RCV Id: RCV000122583

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317693.1:p.Gly28Ala
CA232376
NM_001330764.2:c.83G>C