Canonical Allele Identifier: PA2826410578
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu1174Asp
CA2005539
NM_001256850.1:c.3522A>C
CA349483110
NM_001256850.1:c.3522A>T