Canonical Allele Identifier: PA102713
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 4178
ClinVar RCV Id: RCV000004395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120679.1:p.Arg764Gln
CA253035
NM_001127207.2:c.2291G>A