Canonical Allele Identifier: PA140935
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47414
ClinVar RCV Id: RCV000040684 RCV000082434 RCV000277428 RCV000280746 RCV000316062 RCV000369656 RCV000373068 RCV000620318 RCV000852805 RCV001082278 RCV001798183
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn27520Lys
CA140931
NM_001267550.2:c.82560C>A
CA349572896
NM_001267550.2:c.82560C>G