Canonical Allele Identifier: PA132269
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43193
ClinVar RCV Id: RCV000036097 RCV000263497 RCV000316472 RCV000354842 RCV001041392 RCV001831632
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Gly961Asp
CA132268
NM_000260.4:c.2882G>A