Canonical Allele Identifier: PA2825353334
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 328730
ClinVar RCV Id: RCV000369500
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026896.3:p.His27Leu
CA10642561
NM_001031726.4:c.80A>T