Canonical Allele Identifier: PA2826674449
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2662190
ClinVar RCV Id: RCV003443685

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269858.1:p.Gln5His
CA9351914
NM_001282929.1:c.15G>C
CA405143304
NM_001282929.1:c.15G>T