Canonical Allele Identifier: PA2573206063
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1463860
ClinVar RCV Id: RCV001975307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Arg99Gly
CA386304039
NM_001354304.2:c.295A>G