Canonical Allele Identifier: PA2825629552
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2074839
ClinVar RCV Id: RCV002963083

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120679.1:p.Thr176Ile
CA2097605
NM_001127207.2:c.527C>T