Canonical Allele Identifier: PA2828806732
Gene: CACNG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2661916
ClinVar RCV Id: RCV003441170
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365980.1:p.Ala174Thr
CA323997759
NM_001379051.1:c.520G>A