Canonical Allele Identifier: PA105642
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102717
ClinVar RCV Id: RCV000088965 RCV003474692
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gly171Ala
CA229599
NM_000277.3:c.512G>C