ClinGen Allele Registry
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Canonical Allele Identifier:
PA645477870
Gene: SMARCE1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
407076
ClinVar RCV Id:
RCV000474770
RCV000575784
RCV003151775
RCV003409621
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_003070.3:p.Glu359del
CA8545070
NM_003079.5:c.1076_1078del