Canonical Allele Identifier: PA2580369197
Gene: SIM2 HGNC NCBI
ClinVar RCV:
RCV004236732
ClinVar Variation:
2402779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_033664.2:p.Val269Met
CA320384808
NM_009586.5:c.805G>A