Canonical Allele Identifier: PA2828189628
Gene: C1QTNF6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2225782
ClinVar RCV Id: RCV004086938

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352807.1:p.Met19Ile
CA10217017
NM_001365878.1:c.57G>T
CA411432325
NM_001365878.1:c.57G>C
CA411432326
NM_001365878.1:c.57G>A