Canonical Allele Identifier: PA139567
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46935
ClinVar RCV Id: RCV000040205 RCV000082399 RCV000279186 RCV000336318 RCV000337656 RCV000294379 RCV000385921 RCV000620121 RCV001086509 RCV001798149 RCV004541151
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val13500Phe
CA139563
NM_001267550.2:c.40498G>T