Canonical Allele Identifier: PA2826426236
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 516026

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asn30321Asp
CA1986859
NM_001256850.1:c.90961A>G