Canonical Allele Identifier: PA309699
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202594
ClinVar RCV Id: RCV000551399 RCV000726155 RCV003987429
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val11287Ala
CA309698
NM_001256850.1:c.33860T>C