Canonical Allele Identifier: PA105003
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 92731
ClinVar RCV Id: RCV000078506 RCV000150075 RCV000622360 RCV003915048
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ala403Val
CA273106
NM_000277.3:c.1208C>T