Canonical Allele Identifier: PA916037468
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 587
ClinVar RCV Id: RCV000000618 RCV000078522 RCV003415608
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Arg158Gln
CA251530
NM_001354304.2:c.473G>A