Canonical Allele Identifier: PA140758
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47348
ClinVar RCV Id: RCV000040618 RCV000172252 RCV000303107 RCV000271372 RCV000365850 RCV000306562 RCV000400010 RCV001085393 RCV003448252 RCV004541177 RCV003486598
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp22990Val
CA140756
NM_133378.4:c.68969A>T