Canonical Allele Identifier: PA645410379
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu19657Asp
CA1992749
NM_001267550.2:c.58971A>C
CA349500202
NM_001267550.2:c.58971A>T