Canonical Allele Identifier: PA238257
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192074
ClinVar RCV Id: RCV000172465 RCV001078603
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr2257Ser
CA238254
NM_133378.4:c.6770C>G
CA349682052
NM_133378.4:c.6769A>T