Canonical Allele Identifier: PA106693
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 603
ClinVar RCV Id: RCV000000634 RCV000078531
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Tyr277Asp
CA251534
NM_000277.3:c.829T>G