Canonical Allele Identifier: PA2825629835
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 334295
ClinVar RCV Id: RCV000302549 RCV000594612 RCV003912407
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120679.1:p.Thr399Met
CA2097812
NM_001127207.2:c.1196C>T