Canonical Allele Identifier: PA2826428973
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405103
ClinVar RCV Id: RCV000467853
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Tyr33701Cys
CA16610281
NM_001256850.1:c.101102A>G