Canonical Allele Identifier: PA295773
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 137839

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile6004Val
CA295771
NM_001256850.1:c.18010A>G