Canonical Allele Identifier: PA139839
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47042
ClinVar RCV Id: RCV000040312 RCV000284717 RCV000288386 RCV000324575 RCV000339767 RCV000404730 RCV000539364 RCV000770017 RCV001703901 RCV002426575 RCV004541159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile15147Thr
CA139836
NM_001256850.1:c.45440T>C