Canonical Allele Identifier: PA915980877
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43162
ClinVar RCV Id: RCV000036066 RCV000664583 RCV000933794 RCV001276681
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg623His
CA132227
NM_001127180.2:c.1868G>A