Canonical Allele Identifier: PA645477872
Gene: SMARCE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 407068
ClinVar RCV Id: RCV000457140 RCV001017267 RCV003932709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003070.3:p.Glu365Asp
CA8545063
NM_003079.5:c.1095G>C
CA399361459
NM_003079.5:c.1095G>T