Canonical Allele Identifier: PA2826050982
Gene: CCM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1305187
ClinVar RCV Id: RCV001773897
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161407.1:p.Lys10Asn
CA367423701
NM_001167935.1:c.30G>C
CA367423702
NM_001167935.1:c.30G>T