Canonical Allele Identifier: PA106571
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102625
ClinVar RCV Id: RCV000088867 RCV001260324
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ser67Pro
CA229481
NM_000277.3:c.199T>C