Canonical Allele Identifier: PA260568
Gene: COL6A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36916
ClinVar RCV Id: RCV003764644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001840.3:p.Val619_Ile620del
CA260566
NM_001849.4:c.1856_1861del