Canonical Allele Identifier: PA1139675122
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 853296
ClinVar RCV Id: RCV001058079

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn1633Asp
CA044154
NM_000257.4:c.4897A>G