Canonical Allele Identifier: PA2826292598
Gene: ZNF497 HGNC NCBI
ClinVar RCV:
RCV004184699
ClinVar Variation:
2347180
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193938.1:p.Pro273Thr
CA9714396
NM_001207009.2:c.817C>A