Canonical Allele Identifier: PA312805
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1453298
ClinVar RCV Id: RCV002000227
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Glu205Asp
CA312804
NM_000277.3:c.615G>C
CA386296707
NM_000277.3:c.615G>T