Canonical Allele Identifier: PA2825353356
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 469655
ClinVar RCV Id: RCV000550717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026896.3:p.Val41Ile
CA9351983
NM_001031726.4:c.121G>A