Canonical Allele Identifier: PA2830432898
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2949784
ClinVar RCV Id: RCV003804950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937820.1:p.Leu312Pro
CA353561791
NM_198177.3:c.935T>C