Canonical Allele Identifier: PA658827659
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 557654
ClinVar RCV Id: RCV000673822

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Asn106Lys
CA381931114
NM_000260.4:c.318C>A
CA381931115
NM_000260.4:c.318C>G