Canonical Allele Identifier: PA140007
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47101
ClinVar RCV Id: RCV000040371 RCV000555854 RCV000726968 RCV000764327
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile16739Thr
CA140004
NM_001256850.1:c.50216T>C