Canonical Allele Identifier: PA658807800
Gene: SMARCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 521357
ClinVar RCV Id: RCV000623090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003061.3:p.Val1198Gly
CA372788932
NM_003070.5:c.3593T>G