Canonical Allele Identifier: PA2830433696
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1716465
ClinVar RCV Id: RCV002303514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937821.2:p.Pro329Ala
CA353559954
NM_198178.3:c.985C>G