Canonical Allele Identifier: PA2826427701
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332698
ClinVar RCV Id: RCV000264386 RCV000272777 RCV000308202 RCV000327987 RCV000362783 RCV000518469
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr32455Asn
CA1985774
NM_001256850.1:c.97364C>A