Canonical Allele Identifier: PA109031
Gene: SMC1A HGNC NCBI

Linked Data

ClinVar Variation Id: 159956
ClinVar RCV Id: RCV000147566
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006297.2:p.Tyr1085Cys
CA272574
NM_006306.4:c.3254A>G