Canonical Allele Identifier: PA2825629413
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 260337

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120679.1:p.Ala43Thr
CA2097561
NM_001127207.2:c.127G>A