Canonical Allele Identifier: PA2830433697
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1722868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937821.2:p.Pro329Leu
CA353559958
NM_198178.3:c.986C>T