Canonical Allele Identifier: PA2826674542
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2195733
ClinVar RCV Id: RCV002628903
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269859.1:p.Ala52Asp
CA405142606
NM_001282930.3:c.155C>A