Canonical Allele Identifier: PA2829436948
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47249
ClinVar RCV Id: RCV000040519 RCV000618423 RCV000462522 RCV001507592 RCV003989305
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Gly13318Arg
CA140455
NM_003319.4:c.39952G>A
CA349424385
NM_003319.4:c.39952G>C