Canonical Allele Identifier: PA2825105583
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2949784
ClinVar RCV Id: RCV003804950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000239.1:p.Leu227Pro
CA353561791
NM_000248.4:c.680T>C