Canonical Allele Identifier: PA105279
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102703
ClinVar RCV Id: RCV000088951 RCV000148722
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Asn167Ser
CA229585
NM_000277.3:c.500A>G
CA2837240917
NM_000277.3:c.500_504delinsGCTAT