Canonical Allele Identifier: PA916037705
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 92753
ClinVar RCV Id: RCV000078538 RCV000150082
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Ala309Val
CA220592
NM_001354304.2:c.926C>T