Canonical Allele Identifier: PA2826674578
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2961847
ClinVar RCV Id: RCV003822493
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269860.1:p.Ala29Ser
CA405142967
NM_001282931.3:c.85G>T