Canonical Allele Identifier: PA238251
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192073

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn2309Lys
CA238249
NM_001267550.2:c.6927T>A
CA349681409
NM_001267550.2:c.6927T>G