Canonical Allele Identifier: PA2827882153
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1313766

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341535.1:p.Pro485Ser
CA2490678
NM_001354606.2:c.1453C>T