Canonical Allele Identifier: PA2830203986
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535257
ClinVar RCV Id: RCV000643126

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Leu32222Phe
CA1985433
NM_133378.4:c.96664C>T