Canonical Allele Identifier: PA229890
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102922
ClinVar RCV Id: RCV000089189 RCV001199991
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Phe327Leu
CA229889
NM_000277.3:c.981T>G
CA386493507
NM_000277.3:c.981T>A
CA386493511
NM_000277.3:c.979T>C