Canonical Allele Identifier: PA309779
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202620
ClinVar RCV Id: RCV000724877 RCV001082051 RCV000241687 RCV001798649 RCV002282012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val12189Ile
CA309778
NM_001256850.1:c.36565G>A