Canonical Allele Identifier: PA2828795480
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 198451
ClinVar RCV Id: RCV000179808 RCV000416151 RCV001082663 RCV001147861 RCV001147862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365544.1:p.Ser117Arg
CA203454
NM_001378615.1:c.351T>G
CA356408266
NM_001378615.1:c.349A>C
CA356408272
NM_001378615.1:c.351T>A