Canonical Allele Identifier: PA916065648
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178209

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.His6770Arg
CA181794
NM_133437.4:c.20309A>G