Canonical Allele Identifier: PA2825105558
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2005454
ClinVar RCV Id: RCV002821038

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000239.1:p.Phe190Ser
CA353561521
NM_000248.4:c.569T>C