Canonical Allele Identifier: PA105416
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 617
ClinVar RCV Id: RCV000000648 RCV000088815 RCV000401074 RCV003415609
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Asp415Asn
CA114364
NM_000277.3:c.1243G>A