Canonical Allele Identifier: PA2830195816
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202308

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Lys14232Asn
CA309040
NM_133378.4:c.42696A>T
CA349596373
NM_133378.4:c.42696A>C