Canonical Allele Identifier: PA2580231032
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1810384
ClinVar RCV Id: RCV002509871
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Ala104Val
CA386304006
NM_001354304.2:c.311C>T