Canonical Allele Identifier: PA279576
Gene: SMC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 217799
ClinVar RCV Id: RCV000201864
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005436.1:p.Phe47Leu
CA279574
NM_005445.4:c.139T>C
CA378369824
NM_005445.4:c.141T>A
CA378369825
NM_005445.4:c.141T>G