Canonical Allele Identifier: PA645411147
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404901
ClinVar RCV Id: RCV000457151 RCV002469152 RCV001721495 RCV002339117
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Met26362Thr
CA1989527
NM_001267550.2:c.79085T>C