Canonical Allele Identifier: PA2829651538
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1716465
ClinVar RCV Id: RCV002303514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006713.1:p.Pro491Ala
CA353559954
NM_006722.2:c.1471C>G