Canonical Allele Identifier: PA2828788265
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 744
ClinVar RCV Id: RCV000000780 RCV000445290 RCV001269034 RCV003234885 RCV003764503 RCV004532267
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365546.1:p.Arg1479Cys
CA114471
NM_001378617.1:c.4435C>T