Canonical Allele Identifier: PA139383
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46860
ClinVar RCV Id: RCV000040130 RCV000241648 RCV000474330 RCV001281444 RCV004534888 RCV001798143
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr9485Met
CA139379
NM_133378.4:c.28454C>T