Canonical Allele Identifier: PA2826424377
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467590

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val27360Ile
CA1988393
NM_001256850.1:c.82078G>A