Canonical Allele Identifier: PA311140
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203067

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser32578Arg
CA311139
NM_001256850.1:c.97734T>A
CA349417045
NM_001256850.1:c.97734T>G
CA349417051
NM_001256850.1:c.97732A>C