Canonical Allele Identifier: PA2826765369
Gene: SMARCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1299136
ClinVar RCV Id: RCV001727466
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276325.1:p.Gly1164Arg
CA372788687
NM_001289396.1:c.3490G>A
CA372788688
NM_001289396.1:c.3490G>C