Canonical Allele Identifier: PA2829651539
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1722868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006713.1:p.Pro491Leu
CA353559958
NM_006722.2:c.1472C>T