Canonical Allele Identifier: PA2573194403
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1682823
ClinVar RCV Id: RCV002237729
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269860.1:p.Thr38Met
CA9351891
NM_001282931.3:c.113C>T