Canonical Allele Identifier: PA2827313602
Gene: SMARCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1946191
ClinVar RCV Id: RCV002658722
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317368.1:p.Gly23Val
CA400601657
NM_001330439.1:c.68G>T