Canonical Allele Identifier: PA106509
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102899
ClinVar RCV Id: RCV000089162 RCV000552302
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ser310Phe
CA229855
NM_000277.3:c.929C>T