Canonical Allele Identifier: PA311911
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203282
ClinVar RCV Id: RCV000543382 RCV000764349 RCV001508476
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg6369Gln
CA311910
NM_001256850.1:c.19106G>A