Allele Registry

Canonical Allele Identifier: PA210808

Gene: CARTPT HGNC NCBI

ClinVar RCV:

RCV000023199

ClinVar Variation:

6993

HGVS (amino-acid)	Matching Registered Transcripts
NP_004282.1:p.Leu61Phe	CA210807 NM_004291.4:c.183G>C CA360104558 NM_004291.4:c.183G>T