Canonical Allele Identifier: PA181696
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178184
ClinVar RCV Id: RCV000154912 RCV000172232 RCV000260853 RCV000297223 RCV000314942 RCV000346437 RCV000391203 RCV000619231 RCV001082864 RCV003149944
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly25963Ser
CA181694
NM_001256850.1:c.77887G>A