Canonical Allele Identifier: PA645410577
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332811
ClinVar RCV Id: RCV000279668 RCV000280410 RCV000319635 RCV000351056 RCV000400184
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu21373Phe
CA1991949
NM_001267550.2:c.64119A>C
CA349443770
NM_001267550.2:c.64119A>T