Canonical Allele Identifier: PA2826429556
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 284110
ClinVar RCV Id: RCV000380276
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp34324Gly
CA10604691
NM_001256850.1:c.102971A>G