Canonical Allele Identifier: PA140436
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47243
ClinVar RCV Id: RCV000040513 RCV000266781 RCV000269962 RCV000323852 RCV000384336 RCV000617644 RCV000327353 RCV000456180 RCV001703904
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val22300Ile
CA140433
NM_001267550.2:c.66898G>A