Canonical Allele Identifier: PA916014068
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 286392
ClinVar RCV Id: RCV000304840 RCV000468820 RCV001126321 RCV001848060 RCV003323494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269860.1:p.Val41Met
CA9351885
NM_001282931.3:c.121G>A