Canonical Allele Identifier: PA174318
Gene: C2CD6 HGNC NCBI

Linked Data

ClinVar Variation Id: 161549
ClinVar RCV Id: RCV000149084
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161693.1:p.Leu1752Ser
CA174317
NM_001168221.2:c.5255T>C