Canonical Allele Identifier: PA140057
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47117
ClinVar RCV Id: RCV000040387 RCV000768980 RCV001130203 RCV001130204 RCV001130205 RCV001130206 RCV001130207 RCV001703902 RCV002433518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala18981Val
CA140053
NM_001267550.2:c.56942C>T