Canonical Allele Identifier: PA2825629680
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1390090
ClinVar RCV Id: RCV001890827
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120679.1:p.Asn255Ser
CA350498001
NM_001127207.2:c.764A>G