Canonical Allele Identifier: PA2825138234
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 987907
ClinVar RCV Id: RCV001269313

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Arg400Ser
CA16020967
NM_000277.3:c.1200G>T
CA386493118
NM_000277.3:c.1200G>C