Canonical Allele Identifier: PA645508703
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 334295
ClinVar RCV Id: RCV000302549 RCV000594612 RCV003912407
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054859.2:p.Thr399Met
CA2097812
NM_014140.4:c.1196C>T