Canonical Allele Identifier: PA2826369755
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2195733
ClinVar RCV Id: RCV002628903
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242976.1:p.Ala116Asp
CA405142606
NM_001256047.2:c.347C>A