Canonical Allele Identifier: PA2830059729
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_113636.2:p.His27Leu
CA10642561
NM_031448.6:c.80A>T