Canonical Allele Identifier: PA916065942
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238788
ClinVar RCV Id: RCV000231241 RCV001131398 RCV001131394 RCV001131396 RCV001131395 RCV001131397
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Thr7281Met
CA1994807
NM_133437.4:c.21842C>T