Canonical Allele Identifier: PA267676
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 120287
ClinVar RCV Id: RCV000106368
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.His271Leu
CA267675
NM_000277.3:c.812A>T