Canonical Allele Identifier: PA145388
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 88865
ClinVar RCV Id: RCV000074454 RCV000074453 RCV000493663
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242976.1:p.Ala52Pro
CA145387
NM_001256047.2:c.154G>C