Canonical Allele Identifier: PA229657
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102759
ClinVar RCV Id: RCV000089009 RCV001071178
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Glu205Lys
CA229656
NM_000277.3:c.613G>A