Canonical Allele Identifier: PA141578
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47643
ClinVar RCV Id: RCV000040912 RCV000082468 RCV000621955 RCV000852778 RCV001131352 RCV001131354 RCV001082939 RCV001131353 RCV001131350 RCV001131351 RCV001798210
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg33964His
CA141574
NM_001267550.2:c.101891G>A