Canonical Allele Identifier: PA2825138341
Gene: PAX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2683957
ClinVar RCV Id: RCV003484558

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000269.3:p.Arg71Met
CA378257764
NM_000278.5:c.212G>T