Canonical Allele Identifier: PA2826917692
Gene: RASL12 HGNC NCBI

Linked Data

ClinVar Variation Id: 3151910
ClinVar RCV Id: RCV004438778
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001294859.1:p.Arg106His
CA7613670
NM_001307930.2:c.317G>A