Canonical Allele Identifier: PA916030558
Gene: FAM114A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 92026
ClinVar RCV Id: RCV000122583

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337563.1:p.Gly37Ala
CA232376
NM_001350634.2:c.110G>C