Canonical Allele Identifier: PA2825137874
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1514901
ClinVar RCV Id: RCV002029638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Asn61Ser
CA386304246
NM_000277.3:c.182A>G