Canonical Allele Identifier: PA2829411501
Gene: SMARCD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2690049
ClinVar RCV Id: RCV003493165
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003067.3:p.Pro85Ser
CA6561018
NM_003076.5:c.253C>T