Canonical Allele Identifier: PA645381789
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu9687Ala
CA1998531
NM_133378.4:c.29060A>C