Canonical Allele Identifier: PA139756
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_001254479.2:p.Val15750Ile
CA139752
NM_001267550.2:c.47248G>A