Canonical Allele Identifier: PA229428
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102586
ClinVar RCV Id: RCV000088825 RCV000169393
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ala434Asp
CA229427
NM_000277.3:c.1301C>A