Canonical Allele Identifier: PA2573230041
Gene: MCM3AP HGNC NCBI

Linked Data

ClinVar Variation Id: 1504472
ClinVar RCV Id: RCV002047813

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003897.2:p.Arg976Cys
CA10076688
NM_003906.5:c.2926C>T