Canonical Allele Identifier: PA105773
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 92744
ClinVar RCV Id: RCV000078524 RCV000150088
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.His170Asp
CA273111
NM_000277.3:c.508C>G