Canonical Allele Identifier: PA2825629522
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1009287

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120679.1:p.Ala150Ser
CA2097594
NM_001127207.2:c.448G>T