Canonical Allele Identifier: PA2829436957
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467400
ClinVar RCV Id: RCV000532135 RCV001131635 RCV001131637 RCV001131639 RCV001584289 RCV001131636 RCV001131638 RCV001170576
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Val13339Met
CA1991353
NM_003319.4:c.40015G>A