Canonical Allele Identifier: PA2827882784
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2922092
ClinVar RCV Id: RCV003785306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341537.1:p.His344Leu
CA353559359
NM_001354608.2:c.1031A>T