Canonical Allele Identifier: PA1139710443
Gene: SMC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 816880
ClinVar RCV Id: RCV001007881
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005436.1:p.Lys1034Arg
CA378394461
NM_005445.4:c.3101A>G