Canonical Allele Identifier: PA2825105730
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1716465
ClinVar RCV Id: RCV002303514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000239.1:p.Pro391Ala
CA353559954
NM_000248.4:c.1171C>G