Canonical Allele Identifier: PA915980655
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43327
ClinVar RCV Id: RCV000036233 RCV000515404 RCV000667735 RCV000724325 RCV001003080 RCV001835646 RCV003389445
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Gly214Arg
CA278709
NM_001127180.2:c.640G>A
CA381932112
NM_001127180.2:c.640G>C