Canonical Allele Identifier: PA140546
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47278
ClinVar RCV Id: RCV000040548 RCV000725637 RCV001080058 RCV001170571 RCV002326749 RCV004534923
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Phe21660Leu
CA140543
NM_001256850.1:c.64980C>A
CA349665913
NM_001256850.1:c.64980C>G
CA349665929
NM_001256850.1:c.64978T>C