Canonical Allele Identifier: PA2825105551
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 900358

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000239.1:p.Asn180Lys
CA353561440
NM_000248.4:c.540C>A
CA353561441
NM_000248.4:c.540C>G