Canonical Allele Identifier: PA2826429005
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 959891
ClinVar RCV Id: RCV001233323
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser33727Pro
CA349407031
NM_001256850.1:c.101179T>C