Canonical Allele Identifier: PA344689
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47688
ClinVar RCV Id: RCV000040957 RCV000204885 RCV002408536 RCV004537121 RCV003137574
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr32519Met
CA344687
NM_133378.4:c.97556C>T