Canonical Allele Identifier: PA105299
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102765
ClinVar RCV Id: RCV000089015 RCV000668775
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Asn207Ser
CA229665
NM_000277.3:c.620A>G