Canonical Allele Identifier: PA105719
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102480
ClinVar RCV Id: RCV000088711 RCV001543645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gly344Arg
CA229287
NM_000277.3:c.1030G>C