Canonical Allele Identifier: PA270099
Gene: MERTK HGNC NCBI

Linked Data

ClinVar Variation Id: 143138

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006334.2:p.Gly484Ser
CA270098
NM_006343.3:c.1450G>A