Canonical Allele Identifier: PA229798
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102858
ClinVar RCV Id: RCV000089119 RCV001375900
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Met276Arg
CA229797
NM_000277.3:c.827T>G