Canonical Allele Identifier: PA2830198966
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 497334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Pro21657Leu
CA1990474
NM_133378.4:c.64970C>T