Canonical Allele Identifier: PA2825627679
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43291
ClinVar RCV Id: RCV000036196 RCV000668897 RCV001069199 RCV001826553 RCV003323370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg1835Trp
CA278686
NM_001127180.2:c.5503C>T