Canonical Allele Identifier: PA2826420612
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467397
ClinVar RCV Id: RCV000538703 RCV003486870
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg20679Cys
CA1991397
NM_001256850.1:c.62035C>T