Canonical Allele Identifier: PA2830358755
Gene: FAM151A HGNC NCBI

Linked Data

ClinVar Variation Id: 3091908
ClinVar RCV Id: RCV004378767
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_788954.2:p.Ile447Phe
CA340442329
NM_176782.3:c.1339A>T