Canonical Allele Identifier: PA1139736134
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 991594
ClinVar RCV Id: RCV001279832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054859.2:p.Gln128Glu
CA2097587
NM_014140.4:c.382C>G