Canonical Allele Identifier: PA2829651291
Gene: MITF HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006713.1:p.Ser350Pro
CA123830
NM_006722.2:c.1048T>C