Canonical Allele Identifier: PA891865375
Gene: PAX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156301
ClinVar RCV Id: RCV000144385 RCV000504921 RCV001085420 RCV004544325
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003981.3:p.Ala334Val
CA233182
NM_003990.5:c.1001C>T