Canonical Allele Identifier: PA2827556048
Gene: FAM114A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 92026
ClinVar RCV Id: RCV000122583

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337564.1:p.Gly235Ala
CA232376
NM_001350635.3:c.704G>C