Canonical Allele Identifier: PA311221
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203094

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile33490Val
CA311220
NM_001256850.1:c.100468A>G