Canonical Allele Identifier: PA2742007408
Gene: SMARCD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2504539
ClinVar RCV Id: RCV003232000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620710.2:p.Met53Thr
CA384786279
NM_139071.3:c.158T>C