Canonical Allele Identifier: PA2826416918
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178210

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Met13886Lys
CA181798
NM_001256850.1:c.41657T>A