Canonical Allele Identifier: PA2825772811
Gene: CCNQ HGNC NCBI

Linked Data

ClinVar Variation Id: 2549409
ClinVar RCV Id: RCV004319743
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124469.1:p.Ala172Gly
CA415088049
NM_001130997.3:c.515C>G