Canonical Allele Identifier: PA302717
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 193778

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu9854Asp
CA302714
NM_001256850.1:c.29562A>T
CA349569435
NM_001256850.1:c.29562A>C