Canonical Allele Identifier: PA272582
Gene: SMC1A HGNC NCBI

Linked Data

ClinVar Variation Id: 159958
ClinVar RCV Id: RCV000147568
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006297.2:p.Val1186Ala
CA272578
NM_006306.4:c.3557T>C