Canonical Allele Identifier: PA2573258170
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1670863
ClinVar RCV Id: RCV002196234

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054859.2:p.Pro166Ser
CA2097600
NM_014140.4:c.496C>T