Canonical Allele Identifier: PA916066287
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202684

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Glu8017Ala
CA309974
NM_133437.4:c.24050A>C