Canonical Allele Identifier: PA2830198568
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467426
ClinVar RCV Id: RCV000547446
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Pro20806Ala
CA349664840
NM_133378.4:c.62416C>G