Canonical Allele Identifier: PA2828206900
Gene: CARD14 HGNC NCBI

Linked Data

ClinVar Variation Id: 844790
ClinVar RCV Id: RCV001047729 RCV002264157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001353314.1:p.Leu162Val
CA401336567
NM_001366385.1:c.484C>G