Canonical Allele Identifier: PA2826428940
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332684
ClinVar RCV Id: RCV003486814 RCV000261720 RCV000265122 RCV000297754 RCV000300611 RCV000357728 RCV002521342
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu33658Asp
CA10612002
NM_001256850.1:c.100974G>C
CA349407515
NM_001256850.1:c.100974G>T