Canonical Allele Identifier: PA104844
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102650
ClinVar RCV Id: RCV000088896 RCV000349567 RCV003915115
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ala104Asp
CA229515
NM_000277.3:c.311C>A