Canonical Allele Identifier: PA2825056435
Gene: FAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1343304
ClinVar RCV Id: RCV001843906
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000128.1:p.Ser169Phe
CA393619863
NM_000137.4:c.506C>T