Canonical Allele Identifier: PA2826411148
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu2195Gly
CA238259
NM_001256850.1:c.6584A>G