Canonical Allele Identifier: PA105854
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102721
ClinVar RCV Id: RCV000088969 RCV000993616
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ile174Thr
CA229604
NM_000277.3:c.521T>C