Canonical Allele Identifier: PA2826369631
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 617481
ClinVar RCV Id: RCV000754614 RCV000821485 RCV001544960 RCV002271579
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242975.1:p.Gly54Glu
CA9351931
NM_001256046.3:c.161G>A