Canonical Allele Identifier: PA916037351
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 805805
ClinVar RCV Id: RCV000993600
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Gln20Pro
CA16020721
NM_001354304.2:c.59A>C
CA2695217178
NM_001354304.2:c.59_60delinsCC