Canonical Allele Identifier: PA1139748911
Gene: SMARCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 913366
ClinVar RCV Id: RCV001166956
ClinVar Variation Id: 1343161
ClinVar RCV Id: RCV001843762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620614.2:p.Met1256Ile
CA4963852
NM_139045.4:c.3768G>A
CA372790155
NM_139045.4:c.3768G>C
CA372790156
NM_139045.4:c.3768G>T