Canonical Allele Identifier: PA2830433187
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1716465
ClinVar RCV Id: RCV002303514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937820.1:p.Pro476Ala
CA353559954
NM_198177.3:c.1426C>G