Canonical Allele Identifier: PA2573180478
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1675469
ClinVar RCV Id: RCV002211198 RCV003155469
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Lys515Asn
CA6197506
NM_001127180.2:c.1545G>T
CA381935824
NM_001127180.2:c.1545G>C