Canonical Allele Identifier: PA2830431561
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1716465
ClinVar RCV Id: RCV002303514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937801.1:p.Pro385Ala
CA353559954
NM_198158.3:c.1153C>G