Canonical Allele Identifier: PA2825629554
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 282581
ClinVar RCV Id: RCV000323953

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120679.1:p.Thr176Arg
CA10604223
NM_001127207.2:c.527C>G