Canonical Allele Identifier: PA2826428978
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238697

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asn33707Lys
CA1985172
NM_001256850.1:c.101121C>A
CA349407154
NM_001256850.1:c.101121C>G