Canonical Allele Identifier: PA916065063
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46967

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Asp5600His
CA139661
NM_133437.4:c.16798G>C