Canonical Allele Identifier: PA105965
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 636
ClinVar RCV Id: RCV000000668 RCV000078516 RCV002251847 RCV003398402 RCV004018528
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ile65Thr
CA251544
NM_000277.3:c.194T>C