Canonical Allele Identifier: PA2573258167
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1397861
ClinVar RCV Id: RCV001922428

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054859.2:p.Glu142Asp
CA2097593
NM_014140.4:c.426G>C
CA350497279
NM_014140.4:c.426G>T