Canonical Allele Identifier: PA645412839
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 286984
ClinVar RCV Id: RCV000267874 RCV000266472 RCV000306527 RCV000303178 RCV000338409 RCV000360232 RCV000642963 RCV002411161
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val35253Met
CA1985216
NM_001267550.2:c.105757G>A