Canonical Allele Identifier: PA2580203089
Gene: SMARCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2307651
ClinVar RCV Id: RCV002884014
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317369.1:p.Pro81Leu
CA8706515
NM_001330440.2:c.242C>T