Canonical Allele Identifier: PA2827882664
Gene: MITF HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341537.1:p.Tyr213Cys
CA16043400
NM_001354608.2:c.638A>G