Canonical Allele Identifier: PA2827881956
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1971795
ClinVar RCV Id: RCV002741009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341535.1:p.Pro271Leu
CA2490479
NM_001354606.2:c.812C>T