Canonical Allele Identifier: PA2826428775
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466738
ClinVar RCV Id: RCV000536908 RCV001722486
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Met33497Thr
CA1985265
NM_001256850.1:c.100490T>C