Canonical Allele Identifier: PA2830194199
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Pro10278Ser
CA1997992
NM_133378.4:c.30832C>T