Canonical Allele Identifier: PA282777
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46666
ClinVar RCV Id: RCV000039936 RCV000247348 RCV000461955 RCV001132026 RCV001132027 RCV001132028 RCV001129325 RCV001129326 RCV001572703 RCV003486572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Met6716Lys
CA282773
NM_001267550.2:c.20147T>A