Canonical Allele Identifier: PA645508719
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 282214
ClinVar RCV Id: RCV000319671 RCV001242768
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054859.2:p.Met922Thr
CA2098300
NM_014140.4:c.2765T>C