Canonical Allele Identifier: PA645508705
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 334299

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054859.2:p.Ala472Thr
CA2097873
NM_014140.4:c.1414G>A