Canonical Allele Identifier: PA2826428422
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1926779

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Leu33149Pro
CA349411890
NM_001256850.1:c.99446T>C