Canonical Allele Identifier: PA2828548374
Gene: SIM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 421271
ClinVar RCV Id: RCV000478425

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361698.1:p.Lys708Arg
CA16618228
NM_001374769.1:c.2123A>G