Canonical Allele Identifier: PA149208
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 96070
ClinVar RCV Id: RCV000082135 RCV002311710 RCV001539376 RCV003231145
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Met2250Ile
CA149206
NM_022455.5:c.6750G>A
CA362325521
NM_022455.5:c.6750G>C
CA362325523
NM_022455.5:c.6750G>T