Canonical Allele Identifier: PA915980839
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 143064
ClinVar RCV Id: RCV000132570
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Gly556Val
CA270005
NM_001127180.2:c.1667G>T