Canonical Allele Identifier: PA2829577233
Gene: SIM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2394658
ClinVar RCV Id: RCV004226198
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005060.1:p.Ser123Asn
CA10019697
NM_005069.6:c.368G>A