Canonical Allele Identifier: PA1139741955
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 987767
ClinVar RCV Id: RCV001269066
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Ser70Phe
CA16020747
NM_001354304.2:c.209C>T