Canonical Allele Identifier: PA2826674452
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1335335
ClinVar RCV Id: RCV001816235 RCV002236177
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269858.1:p.Pro8Ser
CA405143263
NM_001282929.1:c.22C>T