Canonical Allele Identifier: PA2826369605
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 328730
ClinVar RCV Id: RCV000369500
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242975.1:p.His27Leu
CA10642561
NM_001256046.3:c.80A>T