Canonical Allele Identifier: PA2830206635
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535197

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val22999Phe
CA1989872
NM_133378.4:c.68995G>T