Canonical Allele Identifier: PA2826425694
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 497027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asn29549Lys
CA1987281
NM_001256850.1:c.88647T>A
CA349482231
NM_001256850.1:c.88647T>G