Canonical Allele Identifier: PA2826292601
Gene: ZNF497 HGNC NCBI

Linked Data

ClinVar Variation Id: 2298688
ClinVar RCV Id: RCV004147803
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193938.1:p.Ala333Ser
CA407908451
NM_001207009.2:c.997G>T