Canonical Allele Identifier: PA2825105740
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 809507
ClinVar RCV Id: RCV000998101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000239.1:p.Ser405del
CA915942981
NM_000248.4:c.1213_1215del