Canonical Allele Identifier: PA2573062091
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1309834
ClinVar RCV Id: RCV001756902

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Pro1751Thr
CA381952249
NM_000260.4:c.5251C>A