Canonical Allele Identifier: PA2825137846
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 805803
ClinVar RCV Id: RCV000993598
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ser16Tyr
CA16020719
NM_000277.3:c.47C>A