Canonical Allele Identifier: PA2825629685
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 838814
ClinVar RCV Id: RCV001040438

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120679.1:p.Ala256Val
CA2097654
NM_001127207.2:c.767C>T