Canonical Allele Identifier: PA658674834
Gene: SMARCE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 463437
ClinVar RCV Id: RCV000575654 RCV000556662
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003070.3:p.Ala290Thr
CA399363829
NM_003079.5:c.868G>A