Canonical Allele Identifier: PA2826410590
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405080
ClinVar RCV Id: RCV000474791 RCV001662420 RCV002460076 RCV003139641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly1203Ala
CA2005517
NM_001256850.1:c.3608G>C