Canonical Allele Identifier: PA179322
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166318
ClinVar RCV Id: RCV000152504 RCV000232506 RCV000621269 RCV001704105 RCV004544382
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Met1557Ile
CA179317
NM_133379.5:c.4671G>A
CA349462827
NM_133379.5:c.4671G>C
CA349462829
NM_133379.5:c.4671G>T