Canonical Allele Identifier: PA2826369626
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 88865
ClinVar RCV Id: RCV000074454 RCV000074453 RCV000493663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242975.1:p.Ala52Pro
CA145387
NM_001256046.3:c.154G>C