Canonical Allele Identifier: PA220579
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 92737
ClinVar RCV Id: RCV000078515 RCV000721179
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Glu57Lys
CA220578
NM_000277.3:c.169G>A