Canonical Allele Identifier: PA229528
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102661
ClinVar RCV Id: RCV000088908 RCV000672629
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Asp129Gly
CA229527
NM_000277.3:c.386A>G