Canonical Allele Identifier: PA2825629569
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 568780
ClinVar RCV Id: RCV000689239

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120679.1:p.Lys189Glu
CA2097613
NM_001127207.2:c.565A>G