Canonical Allele Identifier: PA229496
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102636
ClinVar RCV Id: RCV000088880 RCV001857429
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Glu78Lys
CA229495
NM_000277.3:c.232G>A