Canonical Allele Identifier: PA2826369630
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 402183
ClinVar RCV Id: RCV000454138 RCV000486662 RCV001095481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242975.1:p.Gly54Val
CA9351930
NM_001256046.3:c.161G>T