Canonical Allele Identifier: PA2580305884
Gene: CARTPT HGNC NCBI

Linked Data

ClinVar Variation Id: 2331196
ClinVar RCV Id: RCV004174848
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004282.1:p.Leu11Ile
CA3298262
NM_004291.4:c.31C>A