Canonical Allele Identifier: PA2826369651
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1682828
ClinVar RCV Id: RCV002237734 RCV003883795
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242975.1:p.Pro74Arg
CA9351910
NM_001256046.3:c.221C>G