Canonical Allele Identifier: PA141534
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47621

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu33301Lys
CA141530
NM_001267550.2:c.99901G>A