Canonical Allele Identifier: PA229444
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102599
ClinVar RCV Id: RCV000088840 RCV001389300
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Leu52Ser
CA229443
NM_000277.3:c.155T>C