Canonical Allele Identifier: PA2741991166
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2662190
ClinVar RCV Id: RCV003443685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_113636.2:p.Gln69His
CA9351914
NM_031448.6:c.207G>C
CA405143304
NM_031448.6:c.207G>T