Canonical Allele Identifier: PA229862
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102903
ClinVar RCV Id: RCV000089167 RCV001857434 RCV002251982
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ala313Val
CA229861
NM_000277.3:c.938C>T