Canonical Allele Identifier: PA915980696
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 306164
ClinVar RCV Id: RCV000295336 RCV000331580 RCV000380951 RCV001465852
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Ala299Thr
CA6197298
NM_001127180.2:c.895G>A