Canonical Allele Identifier: PA645381368
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Pro9687Leu
CA237921
NM_003319.4:c.29060C>T