Canonical Allele Identifier: PA2826726593
Gene: C2CD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 418738

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273506.1:p.Gly1743Cys
CA16619405
NM_001286577.2:c.5227G>T