Canonical Allele Identifier: PA915980601
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 164656
ClinVar RCV Id: RCV000151476 RCV000665283 RCV001054443 RCV001115095 RCV001115096 RCV001115094 RCV001831942
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.His133Asn
CA177366
NM_001127180.2:c.397C>A