Canonical Allele Identifier: PA105585
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 625
ClinVar RCV Id: RCV000000656 RCV000000657 RCV000078503 RCV003914792 RCV003993726
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Glu390Gly
CA114367
NM_000277.3:c.1169A>G