Canonical Allele Identifier: PA2826369726
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 968088
ClinVar RCV Id: RCV001243141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242976.1:p.Met78Ile
CA9351909
NM_001256047.2:c.234G>A
CA405143172
NM_001256047.2:c.234G>T
CA405143174
NM_001256047.2:c.234G>C