Canonical Allele Identifier: PA2825353385
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 183298
ClinVar RCV Id: RCV000162119 RCV000292174 RCV000516097 RCV001231447 RCV003479030
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026896.3:p.Gly42Arg
CA186055
NM_001031726.4:c.124G>A
CA405145441
NM_001031726.4:c.124G>C