Canonical Allele Identifier: PA1139710429
Gene: SMC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 982726
ClinVar RCV Id: RCV001262371
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005436.1:p.Arg1003Cys
CA378394240
NM_005445.4:c.3007C>T