Canonical Allele Identifier: PA2826421610
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47311

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Met22420Val
CA140640
NM_001256850.1:c.67258A>G