Canonical Allele Identifier: PA2825630031
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 426426
ClinVar RCV Id: RCV000489879 RCV000814798 RCV002526018
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120679.1:p.Ile576Thr
CA2097993
NM_001127207.2:c.1727T>C