Canonical Allele Identifier: PA2825138325
Gene: PAX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 155929
ClinVar RCV Id: RCV000144051

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000269.3:p.Arg56Gln
CA170733
NM_000278.5:c.167G>A