Canonical Allele Identifier: PA645498082
Gene: CCN6 HGNC NCBI

Linked Data

ClinVar Variation Id: 355057
ClinVar RCV Id: RCV000301408 RCV000728169 RCV000954665 RCV004022013
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003871.1:p.Pro26Leu
CA3963906
NM_003880.4:c.77C>T