Canonical Allele Identifier: PA104979
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102549
ClinVar RCV Id: RCV000088783 RCV000410586
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ala395Gly
CA286498
NM_000277.3:c.1184C>G