Canonical Allele Identifier: PA2826418460
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165968

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr16819Ala
CA178711
NM_001256850.1:c.50455A>G