Canonical Allele Identifier: PA302479
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191944
ClinVar RCV Id: RCV000172312 RCV000242658 RCV000259186 RCV000313378 RCV000354316 RCV000312071 RCV000366773 RCV000277068 RCV000395819 RCV000768993 RCV001082395 RCV004535173
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Leu16596Pro
CA302477
NM_001256850.1:c.49787T>C