Canonical Allele Identifier: PA106643
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102580
ClinVar RCV Id: RCV000088818 RCV000672448
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Thr418Pro
CA229418
NM_000277.3:c.1252A>C