Canonical Allele Identifier: PA2499245437
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_001269860.1:p.Val47Ala
CA405142691
NM_001282931.3:c.140T>C