Canonical Allele Identifier: PA2825630252
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 495338
ClinVar RCV Id: RCV000586742 RCV001849404
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120679.1:p.Arg764Trp
CA350503975
NM_001127207.2:c.2290C>T