Canonical Allele Identifier: PA2825629511
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1397861
ClinVar RCV Id: RCV001922428
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120679.1:p.Glu142Asp
CA2097593
NM_001127207.2:c.426G>C
CA350497279
NM_001127207.2:c.426G>T