Canonical Allele Identifier: PA658813422
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 496984
ClinVar RCV Id: RCV000596415 RCV001130454 RCV001130455 RCV001130453 RCV001130452 RCV001135523
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val9218Phe
CA1999749
NM_001267550.2:c.27652G>T