Canonical Allele Identifier: PA916050876
Gene: C2CD6 HGNC NCBI

Linked Data

ClinVar Variation Id: 161549
ClinVar RCV Id: RCV000149084

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689738.3:p.Leu555Ser
CA174317
NM_152525.6:c.1664T>C