Canonical Allele Identifier: PA181874
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178235

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu6964Lys
CA181873
NM_133378.4:c.20890G>A