Canonical Allele Identifier: PA105618
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 639
ClinVar RCV Id: RCV000000671 RCV000088878 RCV000672628
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Glu76Gly
CA114373
NM_000277.3:c.227A>G