Canonical Allele Identifier: PA2826674572
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2231424
ClinVar RCV Id: RCV002708058
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269860.1:p.Pro18Ala
CA405143132
NM_001282931.3:c.52C>G