Canonical Allele Identifier: PA2828788195
Gene: CC2D2A HGNC NCBI
ClinVar RCV:
RCV000201637
ClinVar Variation:
217616
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365546.1:p.Gln1448His
CA279430
NM_001378617.1:c.4344A>C
CA356432335
NM_001378617.1:c.4344A>T