Canonical Allele Identifier: PA2741959437
Gene: RASL12 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057647.1:p.Arg82Lys
CA392846792
NM_016563.4:c.245G>A