Canonical Allele Identifier: PA2825137895
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 650381
ClinVar RCV Id: RCV000805522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Asp75Asn
CA6748995
NM_000277.3:c.223G>A