Canonical Allele Identifier: PA645477855
Gene: SMARCE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 225845
ClinVar RCV Id: RCV000211089

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003070.3:p.Tyr73Ser
CA10576104
NM_003079.5:c.218A>C