Canonical Allele Identifier: PA2825629488
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 935546
ClinVar RCV Id: RCV001204167

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120679.1:p.Ile122Val
CA350497138
NM_001127207.2:c.364A>G