Canonical Allele Identifier: PA2825353488
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2038455
ClinVar RCV Id: RCV002894968

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026896.3:p.Pro72Gln
CA405143257
NM_001031726.4:c.215C>A