Canonical Allele Identifier: PA302497
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192001
ClinVar RCV Id: RCV000172373 RCV000412691 RCV001130093 RCV001130094 RCV001130095 RCV001130801 RCV001130800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg9172Trp
CA302495
NM_001256850.1:c.27514C>T