Canonical Allele Identifier: PA141130
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47477
ClinVar RCV Id: RCV000040746 RCV000242549 RCV000262196 RCV000266709 RCV000319678 RCV000354841 RCV000471049 RCV000367586 RCV000768870 RCV000852799 RCV001081488
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ser26897Phe
CA141128
NM_133378.4:c.80690C>T