Canonical Allele Identifier: PA105213
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 612
ClinVar RCV Id: RCV000000643 RCV000088806 RCV003934788
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Arg408Gln
CA229404
NM_000277.3:c.1223G>A