Canonical Allele Identifier: PA105937
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 639999
ClinVar RCV Id: RCV000792932
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ile421Ser
CA16020986
NM_000277.3:c.1262T>G