Canonical Allele Identifier: PA2827882877
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1722868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341537.1:p.Pro440Leu
CA353559958
NM_001354608.2:c.1319C>T