Canonical Allele Identifier: PA915980668
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 178993
ClinVar RCV Id: RCV000155771 RCV000225087 RCV000506187 RCV001254945 RCV001850134 RCV004528892
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Ala230Val
CA278740
NM_001127180.2:c.689C>T