Canonical Allele Identifier: PA105231
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 592
ClinVar RCV Id: RCV000000623 RCV000088813
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Arg413Pro
CA229414
NM_000277.3:c.1238G>C