Canonical Allele Identifier: PA916010811
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 640969
ClinVar RCV Id: RCV000794110

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054859.2:p.Thr163Asn
CA2097599
NM_014140.4:c.488C>A