Canonical Allele Identifier: PA2830204512
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1004601
ClinVar RCV Id: RCV001301330 RCV003135931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly32895Arg
CA349405587
NM_133378.4:c.98683G>A
CA349405590
NM_133378.4:c.98683G>C