Canonical Allele Identifier: PA916010839
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 652582
ClinVar RCV Id: RCV000808161
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054859.2:p.Val433Met
CA2097827
NM_014140.4:c.1297G>A