Canonical Allele Identifier: PA2830431265
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 432664
ClinVar RCV Id: RCV000498171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937801.1:p.His203Arg
CA353561659
NM_198158.3:c.608A>G