Canonical Allele Identifier: PA891854735
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 566403
ClinVar RCV Id: RCV000686205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054859.2:p.Ile259Thr
CA2097657
NM_014140.4:c.776T>C