Canonical Allele Identifier: PA105270
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 92743
ClinVar RCV Id: RCV000078523 RCV000412232
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Asn167Ile
CA220584
NM_000277.3:c.500A>T