Canonical Allele Identifier: PA916047708
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 557654
ClinVar RCV Id: RCV000673822

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Asn95Lys
CA381931114
NM_001369365.1:c.285C>A
CA381931115
NM_001369365.1:c.285C>G