Canonical Allele Identifier: PA2826292577
Gene: ZNF497 HGNC NCBI
ClinVar RCV:
RCV004207775
ClinVar Variation:
2370986
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193938.1:p.Leu61Val
CA9714572
NM_001207009.2:c.181C>G