Canonical Allele Identifier: PA916065016
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46964

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ile5467Thr
CA139649
NM_133437.4:c.16400T>C