Canonical Allele Identifier: PA1139744931
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 217607
ClinVar RCV Id: RCV000201706 RCV000347415 RCV000286210 RCV000474430 RCV000778102 RCV001266486 RCV001542750 RCV002277554 RCV003317149
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365544.1:p.Asp1556Val
CA210318
NM_001378615.1:c.4667A>T