Canonical Allele Identifier: PA311748
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203229
ClinVar RCV Id: RCV000218512 RCV000727092 RCV001082208 RCV002408826
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val4540Met
CA311746
NM_001267550.2:c.13618G>A