Canonical Allele Identifier: PA178541
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165860

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile21727Val
CA178539
NM_001256850.1:c.65179A>G