Canonical Allele Identifier: PA229872
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102910
ClinVar RCV Id: RCV000089174 RCV000666332
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Lys320Asn
CA229871
NM_000277.3:c.960G>C
CA386291550
NM_000277.3:c.960G>T