Canonical Allele Identifier: PA141357
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47562
ClinVar RCV Id: RCV000040831 RCV000252794 RCV000463548 RCV001798201 RCV001703912 RCV004534946
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg32033His
CA141353
NM_001267550.2:c.96098G>A