Canonical Allele Identifier: PA2826369706
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 617481
ClinVar RCV Id: RCV000754614 RCV000821485 RCV001544960 RCV002271579
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242976.1:p.Gly54Glu
CA9351931
NM_001256047.2:c.161G>A