Canonical Allele Identifier: PA229772
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102840
ClinVar RCV Id: RCV000089099 RCV000758096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gln267His
CA229771
NM_000277.3:c.801G>C
CA6748841
NM_000277.3:c.801G>T