Canonical Allele Identifier: PA106860
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 619
ClinVar RCV Id: RCV000000650 RCV000088774
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Val388Met
CA251543
NM_000277.3:c.1162G>A