Canonical Allele Identifier: PA106313
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102766
ClinVar RCV Id: RCV000089016 RCV000411219 RCV001192748
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Pro211Thr
CA229666
NM_000277.3:c.631C>A