Canonical Allele Identifier: PA2828786819
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 194716
ClinVar RCV Id: RCV000193025 RCV000351496 RCV000514696 RCV000404783 RCV001083444
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365546.1:p.Val611Leu
CA206244
NM_001378617.1:c.1831G>C
CA356411981
NM_001378617.1:c.1831G>T