Canonical Allele Identifier: PA2830239226
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 264301
ClinVar RCV Id: RCV000251890 RCV000642979 RCV000827153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Lys21180Asn
CA10587455
NM_133437.4:c.63540A>C
CA349513405
NM_133437.4:c.63540A>T