Canonical Allele Identifier: PA2825353564
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1251967
ClinVar RCV Id: RCV001644555
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026896.3:p.Val111Ala
CA405142691
NM_001031726.4:c.332T>C