Canonical Allele Identifier: PA2826595400
Gene: C1QTNF5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2096932
ClinVar RCV Id: RCV003016437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265360.1:p.Pro201Ser
CA6319911
NM_001278431.2:c.601C>T