Canonical Allele Identifier: PA645412739
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332694
ClinVar RCV Id: RCV000274660 RCV000289473 RCV000327506 RCV000380443 RCV000384361 RCV001565339 RCV002402055
ClinVar Variation Id: 3223359
ClinVar RCV Id: RCV004508714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu34665Val
CA1985506
NM_001267550.2:c.103993C>G
CA2825001004
NM_001267550.2:c.103992_103993delinsGG