Canonical Allele Identifier: PA106703
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102860
ClinVar RCV Id: RCV000089121 RCV000411640
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Tyr277Cys
CA229800
NM_000277.3:c.830A>G