Canonical Allele Identifier: PA2826422131
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332782

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Trp23412Ser
CA1990091
NM_001256850.1:c.70235G>C