Canonical Allele Identifier: PA916067039
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Pro9879Leu
CA237921
NM_133437.4:c.29636C>T