Allele Registry

Canonical Allele Identifier: PA139799

Gene: TTN HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000040295

RCV000172665

RCV000247886

RCV000655929

RCV000768997

RCV001083138

RCV001130555

RCV001131280

RCV001131281

RCV001131282

ClinVar Variation:

47025

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Ile13750Thr	CA139797 NM_133378.4:c.41249T>C