Canonical Allele Identifier: PA2573230035
Gene: MCM3AP HGNC NCBI

Linked Data

ClinVar Variation Id: 1475656
ClinVar RCV Id: RCV001976409 RCV002271312 RCV003170302
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003897.2:p.Gly968Arg
CA10076695
NM_003906.5:c.2902G>A
CA410561654
NM_003906.5:c.2902G>C