Canonical Allele Identifier: PA658667476
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 448821
ClinVar RCV Id: RCV000534861 RCV000710278 RCV002350143
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser28068Thr
CA1988809
NM_001267550.2:c.84203G>C