Canonical Allele Identifier: PA106635
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 628
ClinVar RCV Id: RCV000000660 RCV000078502 RCV000150077 RCV000850463 RCV001280537 RCV003390629 RCV003258654
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Thr380Met
CA114369
NM_000277.3:c.1139C>T