Canonical Allele Identifier: PA311072
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser32987Phe
CA311070
NM_001267550.2:c.98960C>T