Canonical Allele Identifier: PA178863
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166074
ClinVar RCV Id: RCV000152356 RCV000556771 RCV001719941 RCV002381478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala11994Thr
CA178861
NM_001256850.1:c.35980G>A