Canonical Allele Identifier: PA2828830206
Gene: RASL12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2365069
ClinVar RCV Id: RCV004204348
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366358.1:p.Ile216Val
CA7613575
NM_001379429.1:c.646A>G