Canonical Allele Identifier: PA2828189632
Gene: C1QTNF6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2335697
ClinVar RCV Id: RCV004173441
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352807.1:p.Ile71Val
CA10216985
NM_001365878.1:c.211A>G