Canonical Allele Identifier: PA138902
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46667
ClinVar RCV Id: RCV000039937 RCV000082367 RCV000264795 RCV000260706 RCV000319862 RCV000304724 RCV000359492 RCV000852896 RCV001082940 RCV001798132
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile6408Met
CA138899
NM_001256850.1:c.19224A>G