Canonical Allele Identifier: PA229345
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102525
ClinVar RCV Id: RCV000088758 RCV000758106
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Leu367Pro
CA229344
NM_000277.3:c.1100T>C