Canonical Allele Identifier: PA229508
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102645
ClinVar RCV Id: RCV000088890 RCV000763292
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ile95Phe
CA229507
NM_000277.3:c.283A>T