Canonical Allele Identifier: PA913195003
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 619149
ClinVar RCV Id: RCV000758095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Leu62Val
CA16020738
NM_000277.3:c.184C>G