Canonical Allele Identifier: PA2825627218
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1493566
ClinVar RCV Id: RCV001986577
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Asp1575Asn
CA381951033
NM_001127180.2:c.4723G>A