Canonical Allele Identifier: PA2826417225
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229442
ClinVar RCV Id: RCV000214620 RCV002494575 RCV003327384
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala14512Ser
CA10576523
NM_001256850.1:c.43534G>T