Canonical Allele Identifier: PA2830059833
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 31626
ClinVar RCV Id: RCV000024323
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_113636.2:p.Leu121Gln
CA260038
NM_031448.6:c.362T>A