Canonical Allele Identifier: PA645410877
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 264186
ClinVar RCV Id: RCV000246473 RCV001216338 RCV001563433
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg23790Cys
CA1990635
NM_001267550.2:c.71368C>T