Canonical Allele Identifier: PA2826416942
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 548486

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Tyr13950His
CA1995169
NM_001256850.1:c.41848T>C