Canonical Allele Identifier: PA308946
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202271

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro15829Gln
CA308945
NM_001256850.1:c.47486C>A