Canonical Allele Identifier: PA2825630352
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 496639
ClinVar RCV Id: RCV000590927
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120679.1:p.Gly857Glu
CA350504978
NM_001127207.2:c.2570G>A