Canonical Allele Identifier: PA916037805
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102539
ClinVar RCV Id: RCV000088772 RCV001789754 RCV004542806
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Tyr387His
CA229363
NM_001354304.2:c.1159T>C