Canonical Allele Identifier: PA174868
Gene: CCDC171 HGNC NCBI

Linked Data

ClinVar Variation Id: 161830
ClinVar RCV Id: RCV000149366
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775821.2:p.Arg802Trp
CA174867
NM_173550.4:c.2404C>T