Canonical Allele Identifier: PA2829480131
Gene: PAX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2087854
ClinVar RCV Id: RCV003009771

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003980.3:p.Ser66Arg
CA378257728
NM_003989.5:c.196A>C
CA378257734
NM_003989.5:c.198C>A
CA378257735
NM_003989.5:c.198C>G