Canonical Allele Identifier: PA2826674511
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2038455
ClinVar RCV Id: RCV002894968

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269859.1:p.Pro8Gln
CA405143257
NM_001282930.3:c.23C>A