Canonical Allele Identifier: PA2825108940
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2017174
ClinVar RCV Id: RCV002835070

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn224Ser
CA389052288
NM_000257.4:c.671A>G