Canonical Allele Identifier: PA658664602
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466807

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile4282Asn
CA2002659
NM_001267550.2:c.12845T>A