Canonical Allele Identifier: PA2830235143
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_597681.4:p.Pro14501Ala
CA349664840
NM_133437.4:c.43501C>G