Canonical Allele Identifier: PA309900
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202659

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser14305Pro
CA309899
NM_001256850.1:c.42913T>C