Canonical Allele Identifier: PA2826428987
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 661657
ClinVar RCV Id: RCV000819126
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp33712Asn
CA349407130
NM_001256850.1:c.101134G>A