Canonical Allele Identifier: PA208077
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 212475
ClinVar RCV Id: RCV000194123 RCV000534507 RCV001721264 RCV002321778
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg19358Cys
CA208075
NM_001267550.2:c.58072C>T