Canonical Allele Identifier: PA105069
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102693
ClinVar RCV Id: RCV000409986 RCV000088941
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Arg158Trp
CA229570
NM_000277.3:c.472C>T