Canonical Allele Identifier: PA229436
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102594
ClinVar RCV Id: RCV000088833 RCV000666206
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Glu44del
CA229435
NM_000277.3:c.131_133del