Canonical Allele Identifier: PA229485
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102627
ClinVar RCV Id: RCV000088870 RCV001543636
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Arg68Gly
CA229484
NM_000277.3:c.202A>G