Canonical Allele Identifier: PA2573166303
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1419340
ClinVar RCV Id: RCV001931164

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys257Arg
CA389052090
NM_000257.4:c.770A>G