Canonical Allele Identifier: PA139795
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47024
ClinVar RCV Id: RCV000040294 RCV000172666 RCV000244085 RCV000278356 RCV000335718 RCV000284453 RCV000337051 RCV000406708 RCV000768998 RCV001081356 RCV000852850 RCV001358658 RCV004528209
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro14602Ser
CA139792
NM_001256850.1:c.43804C>T