Canonical Allele Identifier: PA2826421605
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332787
ClinVar RCV Id: RCV000263422 RCV000278981 RCV000318621 RCV000324714 RCV000367334
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg22415Ser
CA10611620
NM_001256850.1:c.67243C>A