Canonical Allele Identifier: PA2825105714
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2944207
ClinVar RCV Id: RCV003805957

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000239.1:p.Leu378Pro
CA353559881
NM_000248.4:c.1133T>C