Canonical Allele Identifier: PA2826412719
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404721

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser5200Leu
CA2002023
NM_001256850.1:c.15599C>T