Canonical Allele Identifier: PA2826369638
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 31157
ClinVar RCV Id: RCV000024153 RCV000414809 RCV000528859 RCV001781312 RCV003230372
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242975.1:p.Gly58Arg
CA345637
NM_001256046.3:c.172G>A
CA405143562
NM_001256046.3:c.172G>C