Canonical Allele Identifier: PA2825630361
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1492665
ClinVar RCV Id: RCV002012467
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120679.1:p.Phe863Leu
CA2098253
NM_001127207.2:c.2589T>G
CA350505015
NM_001127207.2:c.2587T>C
CA350505020
NM_001127207.2:c.2589T>A