Canonical Allele Identifier: PA2742026895
Gene: FAM151A HGNC NCBI

Linked Data

ClinVar Variation Id: 2522982
ClinVar RCV Id: RCV004300055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_788954.2:p.Ser448Pro
CA22715739
NM_176782.3:c.1342T>C