Canonical Allele Identifier: PA311267
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203108

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val34002Ile
CA311266
NM_001256850.1:c.102004G>A