Canonical Allele Identifier: PA132292
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43206
ClinVar RCV Id: RCV000036110 RCV000312187 RCV000664879 RCV001073977 RCV001270103 RCV001272512 RCV002496550 RCV004541086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Gly1159Val
CA132291
NM_000260.4:c.3476G>T