Canonical Allele Identifier: PA2573075621
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 347903
ClinVar RCV Id: RCV000310019 RCV000364646 RCV001252766 RCV004530405 RCV000864851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365544.1:p.Thr1401Ser
CA2864351
NM_001378615.1:c.4202C>G
CA356429553
NM_001378615.1:c.4201A>T