Canonical Allele Identifier: PA916066048
Gene: TTN HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Thr7455Ile
CA1994713
NM_133437.4:c.22364C>T