Canonical Allele Identifier: PA2830059827
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1251967
ClinVar RCV Id: RCV001644555
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_113636.2:p.Val111Ala
CA405142691
NM_031448.6:c.332T>C