Canonical Allele Identifier: PA105337
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102667
ClinVar RCV Id: RCV000088915 RCV000546355 RCV002251980 RCV003925098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Asp145Val
CA229539
NM_000277.3:c.434A>T