Canonical Allele Identifier: PA2826151378
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 375215
ClinVar RCV Id: RCV000416300 RCV000416286
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171896.1:p.Lys255Asn
CA16044010
NM_001184967.2:c.765G>C
CA353561637
NM_001184967.2:c.765G>T