Canonical Allele Identifier: PA110936
Gene: FAH HGNC NCBI

Linked Data

ClinVar Variation Id: 11865
ClinVar RCV Id: RCV000012640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000128.1:p.Asn16Ile
CA256099
NM_000137.4:c.47A>T