Canonical Allele Identifier: PA2826414526
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 290470

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Tyr8922His
CA1999737
NM_001256850.1:c.26764T>C