Canonical Allele Identifier: PA2826917689
Gene: RASL12 HGNC NCBI
ClinVar RCV:
RCV004283768
ClinVar Variation:
2508198
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001294859.1:p.Arg63Lys
CA392846792
NM_001307930.2:c.188G>A