Canonical Allele Identifier: PA2826674521
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2876056
ClinVar RCV Id: RCV003743339

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269859.1:p.Asn26Lys
CA9351897
NM_001282930.3:c.78C>G
CA405143008
NM_001282930.3:c.78C>A