Canonical Allele Identifier: PA916037665
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 589
ClinVar RCV Id: RCV000000620 RCV000078534 RCV001265833 RCV003914790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Pro281Leu
CA220589
NM_001354304.2:c.842C>T