Canonical Allele Identifier: PA132224
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43160
ClinVar RCV Id: RCV000036064 RCV000665882 RCV001060312 RCV001826541 RCV002490492 RCV004534753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg616Trp
CA132223
NM_000260.4:c.1846C>T