Canonical Allele Identifier: PA2826428436
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg33164Leu
CA141674
NM_001256850.1:c.99491G>T