Canonical Allele Identifier: PA916065696
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238787
ClinVar RCV Id: RCV000231819
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Thr6893Ser
CA10581867
NM_133437.4:c.20677A>T
CA349618178
NM_133437.4:c.20678C>G