Canonical Allele Identifier: PA105216
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 577
ClinVar RCV Id: RCV000000607 RCV000078507 RCV002512607 RCV002287314 RCV003415607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Arg408Trp
CA251523
NM_000277.3:c.1222C>T