Canonical Allele Identifier: PA141713
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47683
ClinVar RCV Id: RCV000040952 RCV000228793 RCV000275138 RCV000333536 RCV000330183 RCV000369582 RCV000383536 RCV000620982 RCV001081694 RCV001170285
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg32475Cys
CA141711
NM_133378.4:c.97423C>T