Canonical Allele Identifier: PA645510436
Gene: C1QTNF5 HGNC NCBI

Linked Data

ClinVar Variation Id: 438182
ClinVar RCV Id: RCV000505113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056460.1:p.Pro186Ser
CA382968539
NM_015645.5:c.556C>T