Canonical Allele Identifier: PA2828806734
Gene: CACNG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 252658
ClinVar RCV Id: RCV000239025 RCV000727327 RCV003955395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365980.1:p.Ala191Thr
CA10212129
NM_001379051.1:c.571G>A