Canonical Allele Identifier: PA2580223275
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1714193
ClinVar RCV Id: RCV002297173
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Asn376Ser
CA386493256
NM_001354304.2:c.1127A>G