Canonical Allele Identifier: PA181849
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178229
ClinVar RCV Id: RCV000154964 RCV000829061 RCV001134394 RCV001134396 RCV001134393 RCV001134395 RCV001134397
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val10679Ile
CA181848
NM_001267550.2:c.32035G>A