Canonical Allele Identifier: PA140716
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47332
ClinVar RCV Id: RCV000040602 RCV000249030 RCV000471721 RCV000768930 RCV001086359 RCV001128971 RCV001128973 RCV001128972 RCV001128974 RCV001131634 RCV004534927
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gln23324His
CA140713
NM_001256850.1:c.69972A>C
CA349630444
NM_001256850.1:c.69972A>T