Canonical Allele Identifier: PA105091
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102725
ClinVar RCV Id: RCV000088973 RCV001854513
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Arg176Pro
CA229608
NM_000277.3:c.527G>C