Canonical Allele Identifier: PA106625
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102528
ClinVar RCV Id: RCV000088761 RCV000306209
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Thr372Ser
CA229350
NM_000277.3:c.1114A>T