Canonical Allele Identifier: PA2826413819
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404797

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg7498Trp
CA2000625
NM_001256850.1:c.22492C>T