Canonical Allele Identifier: PA2826674464
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1299224
ClinVar RCV Id: RCV001725849 RCV002539775
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269858.1:p.Asn26Asp
CA405143017
NM_001282929.1:c.76A>G