Canonical Allele Identifier: PA2828320028
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 942927
ClinVar RCV Id: RCV001213014
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Lys632Asn
CA381938622
NM_001369365.1:c.1896G>C
CA381938623
NM_001369365.1:c.1896G>T