Canonical Allele Identifier: PA202388
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 196456
ClinVar RCV Id: RCV000177274 RCV000294706 RCV001706133 RCV002294066
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054859.2:p.Arg114His
CA202386
NM_014140.4:c.341G>A