Canonical Allele Identifier: PA2825137850
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 805805
ClinVar RCV Id: RCV000993600
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gln20Pro
CA16020721
NM_000277.3:c.59A>C
CA2695217178
NM_000277.3:c.59_60delinsCC