Canonical Allele Identifier: PA229648
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102755
ClinVar RCV Id: RCV000089004 RCV001543658
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Cys203Trp
CA229647
NM_000277.3:c.609C>G