Canonical Allele Identifier: PA2827313594
Gene: SMARCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1472734
ClinVar RCV Id: RCV001977208
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317368.1:p.Arg6Gln
CA8706541
NM_001330439.1:c.17G>A