Canonical Allele Identifier: PA2826417914
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp15774Asn
CA139896
NM_001256850.1:c.47320G>A