Canonical Allele Identifier: PA310853
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202972
ClinVar RCV Id: RCV000184963 RCV000559240 RCV001721168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg28682Thr
CA310852
NM_001256850.1:c.86045G>C