Canonical Allele Identifier: PA2830432957
Gene: MITF HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937820.1:p.Ser335Pro
CA123830
NM_198177.3:c.1003T>C