Canonical Allele Identifier: PA2826416597
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535373

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val13207Met
CA1995621
NM_001256850.1:c.39619G>A