Canonical Allele Identifier: PA2825056429
Gene: FAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1440957
ClinVar RCV Id: RCV001937019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000128.1:p.Ser165Cys
CA393619841
NM_000137.4:c.494C>G