Canonical Allele Identifier: PA2580172481
Gene: CCDC169 HGNC NCBI

Linked Data

ClinVar Variation Id: 2470484
ClinVar RCV Id: RCV004263927
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185837.1:p.Arg61Cys
CA6949197
NM_001198908.2:c.181C>T