Allele Registry

Canonical Allele Identifier: PA2826369681

Gene: C19orf12 HGNC NCBI

ClinVar Allele:

349629

ClinVar RCV:

RCV000330049

RCV000797968

RCV003144216

ClinVar Variation:

328731

HGVS (amino-acid)	Matching Registered Transcripts
NP_001242976.1:p.Ala23Val	CA9351991 NM_001256047.2:c.68C>T