Canonical Allele Identifier: PA645410019
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404736
ClinVar RCV Id: RCV000477328 RCV000714045 RCV000764334 RCV002446774
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val16601Leu
CA1994514
NM_001267550.2:c.49801G>T
CA349600959
NM_001267550.2:c.49801G>C