Canonical Allele Identifier: PA2825629681
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1484632
ClinVar RCV Id: RCV002005947

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120679.1:p.Asn255Asp
CA350497998
NM_001127207.2:c.763A>G