Canonical Allele Identifier: PA302715
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 193778

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu10171Asp
CA302714
NM_001267550.2:c.30513A>T
CA349569435
NM_001267550.2:c.30513A>C