Canonical Allele Identifier: PA2829790513
Gene: CARD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 999304
ClinVar RCV Id: RCV001295285
ClinVar Variation Id: 2829221
ClinVar RCV Id: RCV003686236
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055774.2:p.Gln365His
CA406664712
NM_014959.5:c.1095A>T
CA406664714
NM_014959.5:c.1095A>C