Canonical Allele Identifier: PA2826417135
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191957

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro14338Leu
CA237963
NM_001256850.1:c.43013C>T