Canonical Allele Identifier: PA2826369659
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2876056
ClinVar RCV Id: RCV003743339
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242975.1:p.Asn90Lys
CA9351897
NM_001256046.3:c.270C>G
CA405143008
NM_001256046.3:c.270C>A