Canonical Allele Identifier: PA2825630321
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2203262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120679.1:p.Arg817Cys
CA350504710
NM_001127207.2:c.2449C>T