Canonical Allele Identifier: PA2825113206
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2853504
ClinVar RCV Id: RCV003747717

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys1668Asn
CA389037155
NM_000257.4:c.5004G>T
CA389037156
NM_000257.4:c.5004G>C