Canonical Allele Identifier: PA2826369603
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 328731
ClinVar RCV Id: RCV000330049 RCV000797968 RCV003144216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242975.1:p.Ala23Val
CA9351991
NM_001256046.3:c.68C>T