Canonical Allele Identifier: PA2826766049
Gene: SMARCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2098131
ClinVar RCV Id: RCV003030793
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276326.1:p.Asn1135Lys
CA372788896
NM_001289397.2:c.3405C>A
CA372788897
NM_001289397.2:c.3405C>G