Canonical Allele Identifier: PA2827882528
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1716465
ClinVar RCV Id: RCV002303514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341536.1:p.Pro475Ala
CA353559954
NM_001354607.2:c.1423C>G