Canonical Allele Identifier: PA206874
Gene: SMARCE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 30316
ClinVar RCV Id: RCV000023251 RCV000193407
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003070.3:p.Tyr73Cys
CA206873
NM_003079.5:c.218A>G