Canonical Allele Identifier: PA141555
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47634
ClinVar RCV Id: RCV000040903 RCV000226035 RCV000620304 RCV001081693 RCV001128954 RCV001131612 RCV001128955 RCV001128953 RCV001131611 RCV001170519
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val32108Met
CA141552
NM_001256850.1:c.96322G>A