Canonical Allele Identifier: PA2829436709
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 497099
ClinVar RCV Id: RCV000598416 RCV000643463 RCV003486887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Lys12970Asn
CA1991578
NM_003319.4:c.38910A>T
CA349429871
NM_003319.4:c.38910A>C