Canonical Allele Identifier: PA105362
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102776
ClinVar RCV Id: RCV000089027 RCV001789760
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Asp222Val
CA229681
NM_000277.3:c.665A>T