Canonical Allele Identifier: PA1139675059
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 928109
ClinVar RCV Id: RCV001191765

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1586Gly
CA389037693
NM_000257.4:c.4757C>G