Canonical Allele Identifier: PA2826428967
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1505993
ClinVar RCV Id: RCV002035882
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Tyr33695Asp
CA60953516
NM_001256850.1:c.101083T>G