Canonical Allele Identifier: PA242899
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 196096
ClinVar RCV Id: RCV000176837 RCV001089335
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly26801Val
CA242898
NM_133378.4:c.80402G>T