Canonical Allele Identifier: PA2826151571
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 809507
ClinVar RCV Id: RCV000998101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171896.1:p.Ser454del
CA915942981
NM_001184967.2:c.1360_1362del