Canonical Allele Identifier: PA2826422897
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405063

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly24875Ser
CA1989460
NM_001256850.1:c.74623G>A