Canonical Allele Identifier: PA2830239900
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467651

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Pro22212Leu
CA1987332
NM_133437.4:c.66635C>T