Canonical Allele Identifier: PA2826413557
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 448774
ClinVar RCV Id: RCV000517328 RCV000525218
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr6945Ser
CA2000953
NM_001256850.1:c.20834C>G
CA349531614
NM_001256850.1:c.20833A>T