Canonical Allele Identifier: PA916037676
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102882
ClinVar RCV Id: RCV000089143 RCV000758136
ClinVar Variation Id: 458082
ClinVar RCV Id: RCV000548849
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Gly289Arg
CA229830
NM_001354304.2:c.865G>C
CA386294434
NM_001354304.2:c.865G>A