Canonical Allele Identifier: PA2830197682
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332811

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Leu18805Phe
CA1991949
NM_133378.4:c.56415A>C
CA349443770
NM_133378.4:c.56415A>T