Canonical Allele Identifier: PA2825056299
Gene: FAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2170717
ClinVar RCV Id: RCV003088675
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000128.1:p.Gly20Asp
CA393615580
NM_000137.4:c.59G>A