Canonical Allele Identifier: PA106849
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102541
ClinVar RCV Id: RCV000088775 RCV001269277
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Val388Leu
CA229366
NM_000277.3:c.1162G>C
CA386493192
NM_000277.3:c.1162G>T