Canonical Allele Identifier: PA2830358768
Gene: FAM151A HGNC NCBI

Linked Data

ClinVar Variation Id: 3091911
ClinVar RCV Id: RCV004378770

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_788954.2:p.Leu578Val
CA866832
NM_176782.3:c.1732T>G