Canonical Allele Identifier: PA2825105737
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2113344
ClinVar RCV Id: RCV003027274

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000239.1:p.Pro398Ser
CA16040406
NM_000248.4:c.1192C>T