Canonical Allele Identifier: PA2826424889
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 518578

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala28210Asp
CA1987895
NM_001256850.1:c.84629C>A