Canonical Allele Identifier: PA2826595366
Gene: C1QTNF5 HGNC NCBI

Linked Data

ClinVar Variation Id: 438182
ClinVar RCV Id: RCV000505113
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265360.1:p.Pro186Ser
CA382968539
NM_001278431.2:c.556C>T