Canonical Allele Identifier: PA645477866
Gene: SMARCE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 407070
ClinVar RCV Id: RCV000472542 RCV000765350 RCV001026703 RCV003409620
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003070.3:p.Lys256Arg
CA8545173
NM_003079.5:c.767A>G