Canonical Allele Identifier: PA645378629
Gene: SMARCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 280814
ClinVar RCV Id: RCV000346583

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003061.3:p.Leu1217Pro
CA10603029
NM_003070.5:c.3650T>C