Canonical Allele Identifier: PA2829517925
Gene: CARTPT HGNC NCBI

Linked Data

ClinVar Variation Id: 3137469
ClinVar RCV Id: RCV004427301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004282.1:p.Ser3Gly
CA3298256
NM_004291.4:c.7A>G