Canonical Allele Identifier: PA2826418734
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg17321Trp
CA60975146
NM_001256850.1:c.51961C>T