Canonical Allele Identifier: PA2826369666
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 31626
ClinVar RCV Id: RCV000024323
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242975.1:p.Cys103Ser
CA260038
NM_001256046.3:c.307T>A
CA405142486
NM_001256046.3:c.308G>C