Canonical Allele Identifier: PA2826674458
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 873517
ClinVar RCV Id: RCV001095768
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269858.1:p.Pro17Thr
CA405143137
NM_001282929.1:c.49C>A