Canonical Allele Identifier: PA1139765285
Gene: CCN6 HGNC NCBI

Linked Data

ClinVar Variation Id: 355057

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937882.2:p.Pro26Leu
CA3963906
NM_198239.2:c.77C>T