Canonical Allele Identifier: PA210808
Gene: CARTPT HGNC NCBI

Linked Data

ClinVar Variation Id: 6993
ClinVar RCV Id: RCV000023199
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Amino-acid Alleles

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