Canonical Allele Identifier: PA2825138317
Gene: PAX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2444301
ClinVar RCV Id: RCV003153099

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000269.3:p.Val42Ala
CA378257578
NM_000278.5:c.125T>C