Canonical Allele Identifier: PA2826151566
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2941566
ClinVar RCV Id: RCV003802588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171896.1:p.Ser446Cys
CA353559992
NM_001184967.2:c.1337C>G