Canonical Allele Identifier: PA2826428442
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1006463
ClinVar RCV Id: RCV001303508

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg33166Lys
CA349411773
NM_001256850.1:c.99497G>A