Canonical Allele Identifier: PA1139675268
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 857012
ClinVar RCV Id: RCV001062605
ClinVar Variation Id: 1388062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn1679Lys
CA389037090
NM_000257.4:c.5037C>G
CA389037091
NM_000257.4:c.5037C>A