Allele Registry

Canonical Allele Identifier: PA2826369626

Gene: C19orf12 HGNC NCBI

ClinVar Allele:

94434

ClinVar RCV:

RCV000074453

RCV000074454

RCV000493663

ClinVar Variation:

88865

HGVS (amino-acid)	Matching Registered Transcripts
NP_001242975.1:p.Ala52Pro	CA145387 NM_001256046.3:c.154G>C