Canonical Allele Identifier: PA2829480405
Gene: PAX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1333274
ClinVar RCV Id: RCV001807962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003981.3:p.Arg59Trp
CA378257683
NM_003990.5:c.175C>T