Canonical Allele Identifier: PA311932
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203288
ClinVar RCV Id: RCV000281508 RCV000296750 RCV000336597 RCV000351488 RCV000399478 RCV001704954
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Lys6806Asn
CA311930
NM_001267550.2:c.20418A>C
CA349544764
NM_001267550.2:c.20418A>T