Canonical Allele Identifier: PA915956287
Gene: C1orf167 HGNC NCBI

Linked Data

ClinVar Variation Id: 292196
ClinVar RCV Id: RCV000345123
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001010881.1:p.Leu1303del
CA10607836
NM_001010881.1:c.3906_3908del
CA886036603
NM_001010881.1:c.3903_3905del