Canonical Allele Identifier: PA309894
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202657
ClinVar RCV Id: RCV000464661 RCV000727858 RCV004525888 RCV002415794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile14198Thr
CA309893
NM_001256850.1:c.42593T>C