Canonical Allele Identifier: PA2826410351
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192093

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala835Asp
CA238319
NM_001256850.1:c.2504C>A