Canonical Allele Identifier: PA2825353553
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 286392
ClinVar RCV Id: RCV000304840 RCV000468820 RCV001126321 RCV001848060 RCV003323494
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026896.3:p.Val105Met
CA9351885
NM_001031726.4:c.313G>A