Canonical Allele Identifier: PA916064662
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 282657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Pro4800Leu
CA1996322
NM_133437.4:c.14399C>T