Allele Registry

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Canonical Allele Identifier: PA2825056597

Gene: FAH HGNC NCBI

Linked Data

ClinVar Variation Id: 884320

ClinVar RCV Id: RCV001115333

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000128.1:p.Gln329His	CA393621702 NM_000137.4:c.987G>C CA393621703 NM_000137.4:c.987G>T