Canonical Allele Identifier: PA2580532541
Gene: FAM151A HGNC NCBI

Linked Data

ClinVar Variation Id: 2373373
ClinVar RCV Id: RCV004210389
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_788954.2:p.Val582Ile
CA866828
NM_176782.3:c.1744G>A