Canonical Allele Identifier: PA645408815
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 283986

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn4421Ser
CA2002605
NM_001267550.2:c.13262A>G