Canonical Allele Identifier: PA2741991171
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2876056
ClinVar RCV Id: RCV003743339
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_113636.2:p.Asn90Lys
CA9351897
NM_031448.6:c.270C>G
CA405143008
NM_031448.6:c.270C>A