Canonical Allele Identifier: PA2826674463
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2876056
ClinVar RCV Id: RCV003743339
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269858.1:p.Asn26Lys
CA9351897
NM_001282929.1:c.78C>G
CA405143008
NM_001282929.1:c.78C>A