Canonical Allele Identifier: PA2829651549
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2113344
ClinVar RCV Id: RCV003027274

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006713.1:p.Pro498Ser
CA16040406
NM_006722.2:c.1492C>T