Canonical Allele Identifier: PA106788
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102726
ClinVar RCV Id: RCV000088975 RCV000534379 RCV000589313 RCV003905086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Val177Met
CA229609
NM_000277.3:c.529G>A