Canonical Allele Identifier: PA2825629495
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 991594
ClinVar RCV Id: RCV001279832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120679.1:p.Gln128Glu
CA2097587
NM_001127207.2:c.382C>G