Canonical Allele Identifier: PA2826421257
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 196058

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg21838Trp
CA242813
NM_001256850.1:c.65512C>T