Canonical Allele Identifier: PA2826491529
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1780433
ClinVar RCV Id: RCV002410026
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Met647Thr
CA349505971
NM_001267550.2:c.1940T>C