Canonical Allele Identifier: PA2741858363
Gene: SMARCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2550652
ClinVar RCV Id: RCV003258366
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317369.1:p.Ala82Thr
CA400601469
NM_001330440.2:c.244G>A