Canonical Allele Identifier: PA140818
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47368
ClinVar RCV Id: RCV000040638 RCV000247997 RCV000643181 RCV000726516 RCV001134832 RCV001134833 RCV001134834 RCV001134830 RCV001134831 RCV001781364 RCV004534931 RCV003149658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly26298Arg
CA140814
NM_001267550.2:c.78892G>A
CA349600710
NM_001267550.2:c.78892G>C