Canonical Allele Identifier: PA2825138086
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2226702
ClinVar RCV Id: RCV002727585
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Met276Leu
CA6748838
NM_000277.3:c.826A>T
CA386294548
NM_000277.3:c.826A>C