Canonical Allele Identifier: PA278708
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43325
ClinVar RCV Id: RCV000036230 RCV000675104 RCV001073506 RCV001275896 RCV001852751 RCV002496555
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Ser211Gly
CA278707
NM_000260.4:c.631A>G