Canonical Allele Identifier: PA2826369673
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2988212
ClinVar RCV Id: RCV003844395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242976.1:p.Ile3Val
CA306789004
NM_001256047.2:c.7A>G