Canonical Allele Identifier: PA106007
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 92747
ClinVar RCV Id: RCV000078527 RCV000150086
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Leu213Pro
CA273109
NM_000277.3:c.638T>C