Canonical Allele Identifier: PA2830200402
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535366

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Phe25190Leu
CA1988949
NM_133378.4:c.75568T>C
CA349568519
NM_133378.4:c.75570T>A
CA349568522
NM_133378.4:c.75570T>G