Canonical Allele Identifier: PA106479
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102786
ClinVar RCV Id: RCV000089037 RCV000190611
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ser231Pro
CA229694
NM_000277.3:c.691T>C