Canonical Allele Identifier: PA2830432167
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1716465
ClinVar RCV Id: RCV002303514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937802.1:p.Pro492Ala
CA353559954
NM_198159.3:c.1474C>G