Canonical Allele Identifier: PA2829448292
Gene: TRRAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2498251
ClinVar RCV Id: RCV003221372 RCV004555908
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003487.1:p.Arg2899Cys
CA368311001
NM_003496.4:c.8695C>T