Canonical Allele Identifier: PA1139677488
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 957900
ClinVar RCV Id: RCV001230968
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Lys2045Asn
CA381935880
NM_000260.4:c.6135G>C
CA381935881
NM_000260.4:c.6135G>T