Canonical Allele Identifier: PA311876
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203270

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Cys6127Gly
CA311874
NM_001267550.2:c.18379T>G