Canonical Allele Identifier: PA311307
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203120

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Met1279Leu
CA311304
NM_001267550.2:c.3835A>T
CA349477727
NM_001267550.2:c.3835A>C