Canonical Allele Identifier: PA658825256
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 553638
ClinVar RCV Id: RCV000669128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gly103Cys
CA6748984
NM_000277.3:c.307G>T