Canonical Allele Identifier: PA2825137858
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2074268
ClinVar RCV Id: RCV002976127
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gly33Val
CA386302590
NM_000277.3:c.98G>T