Canonical Allele Identifier: PA2826425965
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 522707

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp29995Asn
CA1987045
NM_001256850.1:c.89983G>A