Canonical Allele Identifier: PA658665420
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467104

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro13019Leu
CA1996880
NM_001267550.2:c.39056C>T