Canonical Allele Identifier: PA2830201662
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 282539
ClinVar RCV Id: RCV000334287

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Met28069Leu
CA10604211
NM_133378.4:c.84205A>T
CA349496003
NM_133378.4:c.84205A>C