Canonical Allele Identifier: PA132238
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43176
ClinVar RCV Id: RCV000036080 RCV000666826 RCV001112680 RCV001112681 RCV001112682 RCV001276686 RCV001852742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg740Trp
CA132237
NM_000260.4:c.2218C>T