Canonical Allele Identifier: PA2580532529
Gene: FAM151A HGNC NCBI

Linked Data

ClinVar Variation Id: 2296849
ClinVar RCV Id: RCV004140970
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_788954.2:p.Arg430His
CA866939
NM_176782.3:c.1289G>A