Canonical Allele Identifier: PA915980698
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 11852
ClinVar RCV Id: RCV000012626 RCV000036251 RCV000386045 RCV000282374 RCV000337254 RCV000758141 RCV000835045 RCV002490355
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg302His
CA132454
NM_001127180.2:c.905G>A