Canonical Allele Identifier: PA105974
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102622
ClinVar RCV Id: RCV000088864 RCV000803656
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ile65Val
CA229478
NM_000277.3:c.193A>G