Canonical Allele Identifier: PA2826674561
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1879429
ClinVar RCV Id: RCV002511928
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269860.1:p.Ser3Asn
CA9351915
NM_001282931.3:c.8G>A