Allele Registry

Canonical Allele Identifier: PA140522

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000040538

RCV000282806

RCV000307639

RCV000337009

RCV000342426

RCV000405692

RCV000463057

RCV000618829

RCV001093056

RCV001293209

RCV001787841

RCV001798175

RCV004534921

ClinVar Variation:

47268

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Ala21179Pro	CA140519 NM_001256850.1:c.63535G>C