Canonical Allele Identifier: PA1139736096
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 935216
ClinVar RCV Id: RCV001203760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054859.2:p.Ser79Leu
CA350496849
NM_014140.4:c.236C>T