Canonical Allele Identifier: PA229487
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102628
ClinVar RCV Id: RCV000088871 RCV003315609
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Pro69Ser
CA229486
NM_000277.3:c.205C>T