Canonical Allele Identifier: PA104952
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102473
ClinVar RCV Id: RCV000088704 RCV001386152
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ala342Thr
CA229276
NM_000277.3:c.1024G>A