Canonical Allele Identifier: PA916010878
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 827737
ClinVar RCV Id: RCV001027621 RCV001269553 RCV001040718
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054859.2:p.Arg820His
CA2098212
NM_014140.4:c.2459G>A