Canonical Allele Identifier: PA645427751
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 432663
ClinVar RCV Id: RCV000497657 RCV001112405 RCV001112406 RCV001112407 RCV001275538
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Thr2170Ile
CA6199098
NM_000260.4:c.6509C>T