Canonical Allele Identifier: PA658812932
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535545

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn6650Ser
CA2001303
NM_001267550.2:c.19949A>G