Canonical Allele Identifier: PA2826151381
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 432664
ClinVar RCV Id: RCV000498171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171896.1:p.His258Arg
CA353561659
NM_001184967.2:c.773A>G