Canonical Allele Identifier: PA916038012
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 432664
ClinVar RCV Id: RCV000498171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341533.1:p.His316Arg
CA353561659
NM_001354604.2:c.947A>G