Canonical Allele Identifier: PA2825627190
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 991570
ClinVar RCV Id: RCV001279803
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Phe1559Leu
CA381950935
NM_001127180.2:c.4675T>C
CA381950939
NM_001127180.2:c.4677C>A
CA381950940
NM_001127180.2:c.4677C>G