Canonical Allele Identifier: PA2825105735
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2941566
ClinVar RCV Id: RCV003802588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000239.1:p.Ser397Cys
CA353559992
NM_000248.4:c.1190C>G