Canonical Allele Identifier: PA2830059756
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_113636.2:p.Gly54Val
CA9351930
NM_031448.6:c.161G>T