Canonical Allele Identifier: PA105598
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102610
ClinVar RCV Id: RCV000088852 RCV001543635
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Glu56Asp
CA229459
NM_000277.3:c.168G>T
CA386302277
NM_000277.3:c.168G>C