Canonical Allele Identifier: PA2828652839
Gene: ZC3H11A HGNC NCBI
ClinVar RCV:
RCV004481179
ClinVar Variation:
3192241
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363286.1:p.Thr347Ala
CA35718108
NM_001376357.1:c.1039A>G