Canonical Allele Identifier: PA2741906732
Gene: PAX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2683957
ClinVar RCV Id: RCV003484558

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003981.3:p.Arg71Met
CA378257764
NM_003990.5:c.212G>T