Canonical Allele Identifier: PA2825629468
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2151638
ClinVar RCV Id: RCV003078938

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120679.1:p.Pro105Leu
CA2097579
NM_001127207.2:c.314C>T