Canonical Allele Identifier: PA178435
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165722
ClinVar RCV Id: RCV000152186 RCV000618452 RCV001129398 RCV001129395 RCV001129396 RCV003480065 RCV001129397 RCV001129399
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg31349Cys
CA178433
NM_001267550.2:c.94045C>T