Canonical Allele Identifier: PA2826369634
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 855673
ClinVar RCV Id: RCV001060989
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242975.1:p.Gly55Arg
CA405143602
NM_001256046.3:c.163G>C
CA405143604
NM_001256046.3:c.163G>A