Canonical Allele Identifier: PA2741991174
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2987861
ClinVar RCV Id: RCV003841980
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_113636.2:p.Ile96Val
CA405142923
NM_031448.6:c.286A>G