Canonical Allele Identifier: PA658825264
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 552657
ClinVar RCV Id: RCV000667958

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gly148Val
CA16020791
NM_000277.3:c.443G>T