Canonical Allele Identifier: PA111099
Gene: FAH HGNC NCBI

Linked Data

ClinVar Variation Id: 558415
ClinVar RCV Id: RCV000674680

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000128.1:p.Val166Gly
CA7691198
NM_000137.4:c.497T>G