Canonical Allele Identifier: PA645412836
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 262342

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala35246Gly
CA1985217
NM_001267550.2:c.105737C>G