Canonical Allele Identifier: PA2826429112
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2438042
ClinVar RCV Id: RCV003137207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser33844Phe
CA349405208
NM_001256850.1:c.101531C>T