Canonical Allele Identifier: PA139755
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47008
ClinVar RCV Id: RCV000040278 RCV000172668 RCV000262089 RCV000251802 RCV000296178 RCV000331321 RCV000332423 RCV000385584 RCV000769009 RCV000767391 RCV001082393 RCV004534901
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val14109Ile
CA139752
NM_001256850.1:c.42325G>A