Canonical Allele Identifier: PA105373
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102874
ClinVar RCV Id: RCV000089135 RCV000411380
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Asp282Asn
CA229817
NM_000277.3:c.844G>A