Canonical Allele Identifier: PA178485
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 96306
ClinVar RCV Id: RCV000152208 RCV000261192 RCV000332574 RCV000389361 RCV000301222 RCV000467146 RCV000353634 RCV000723763 RCV001170790 RCV004529866 RCV002345399
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Phe25114Leu
CA178482
NM_001256850.1:c.75340T>C
CA349589806
NM_001256850.1:c.75342C>G
CA349589807
NM_001256850.1:c.75342C>A