Canonical Allele Identifier: PA916053395
Gene: CCDC170 HGNC NCBI

Linked Data

ClinVar Variation Id: 792060
ClinVar RCV Id: RCV000975135
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079335.2:p.Ala615Asp
CA4051988
NM_025059.4:c.1844C>A