Canonical Allele Identifier: PA2830194785
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404688
ClinVar RCV Id: RCV000463928 RCV000604586 RCV000714032
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp11712Glu
CA1996010
NM_133378.4:c.35136T>G
CA349653714
NM_133378.4:c.35136T>A