Canonical Allele Identifier: PA105894
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102877
ClinVar RCV Id: RCV000089138 RCV000758133
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ile283Asn
CA229821
NM_000277.3:c.848T>A