Canonical Allele Identifier: PA2825629648
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 964662
ClinVar RCV Id: RCV001238928
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120679.1:p.Val242Ile
CA2097644
NM_001127207.2:c.724G>A