Allele Registry

Canonical Allele Identifier: PA106179

Gene: PAH HGNC NCBI

ClinVar Variation Id: 102859

ClinVar Variation Id: 551519

ClinVar RCV Id: RCV000666601

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Met276Ile	CA229799 NM_000277.3:c.828G>T CA386294546 NM_000277.3:c.828G>C CA386294547 NM_000277.3:c.828G>A