Canonical Allele Identifier: PA2826422969
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405048
ClinVar RCV Id: RCV000464905 RCV000597470 RCV002339120 RCV003330689
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg24987Pro
CA1989422
NM_001256850.1:c.74960G>C