Canonical Allele Identifier: PA2741903492
Gene: MCM3AP HGNC NCBI

Linked Data

ClinVar Variation Id: 2614871
ClinVar RCV Id: RCV003365017
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003897.2:p.Gln1003Arg
CA10076666
NM_003906.5:c.3008A>G