Canonical Allele Identifier: PA2825137978
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1494029
ClinVar RCV Id: RCV001986924 RCV003402026
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.His170Pro
CA16020805
NM_000277.3:c.509A>C