Canonical Allele Identifier: PA2742032789
Gene: ZNF497 HGNC NCBI

Linked Data

ClinVar Variation Id: 2614655
ClinVar RCV Id: RCV004358699

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_940860.2:p.Leu74Val
CA310589904
NM_198458.3:c.220C>G