Canonical Allele Identifier: PA1139736105
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 935546
ClinVar RCV Id: RCV001204167

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054859.2:p.Ile122Val
CA350497138
NM_014140.4:c.364A>G