Canonical Allele Identifier: PA105308
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102617
ClinVar RCV Id: RCV000088859 RCV001389299
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Asn61Asp
CA229470
NM_000277.3:c.181A>G