Canonical Allele Identifier: PA2829651198
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 900358

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006713.1:p.Asn286Lys
CA353561440
NM_006722.2:c.858C>A
CA353561441
NM_006722.2:c.858C>G