Canonical Allele Identifier: PA2829651519
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1313766

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006713.1:p.Pro485Ser
CA2490678
NM_006722.2:c.1453C>T