Canonical Allele Identifier: PA102704
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 4175
ClinVar RCV Id: RCV000004392
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120679.1:p.Arg645Cys
CA253029
NM_001127207.2:c.1933C>T