Canonical Allele Identifier: PA2825115237
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1313976
ClinVar RCV Id: RCV001771207

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Glu513Asp
CA381935798
NM_000260.4:c.1539G>C
CA381935799
NM_000260.4:c.1539G>T