Canonical Allele Identifier: PA2580298576
Gene: MCM3AP HGNC NCBI

Linked Data

ClinVar Variation Id: 2338098
ClinVar RCV Id: RCV002936138
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003897.2:p.Pro972Ser
CA410561600
NM_003906.5:c.2914C>T