Canonical Allele Identifier: PA106992
Gene: CACNG2 HGNC NCBI
ClinVar RCV:
RCV000023217
ClinVar Variation:
30282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006069.1:p.Val143Leu
CA411379456
NM_006078.5:c.427G>T
CA411379461
NM_006078.5:c.427G>C