Canonical Allele Identifier: PA229652
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102757
ClinVar RCV Id: RCV000089006 RCV000993618
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gln20His
CA229651
NM_000277.3:c.60G>C
CA386303792
NM_000277.3:c.60G>T