Canonical Allele Identifier: PA645508692
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 260337

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054859.2:p.Ala43Thr
CA2097561
NM_014140.4:c.127G>A