Canonical Allele Identifier: PA2826607633
Gene: MCM7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2348096
ClinVar RCV Id: RCV004184755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265524.1:p.Met29Val
CA4373978
NM_001278595.2:c.85A>G