Canonical Allele Identifier: PA106781
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102727
ClinVar RCV Id: RCV000088976 RCV000669836 RCV003390790
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Val177Leu
CA229610
NM_000277.3:c.529G>C
CA386297003
NM_000277.3:c.529G>T