Canonical Allele Identifier: PA658830546
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 546459
ClinVar RCV Id: RCV000658339

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Met22Ile
CA391933878
NM_152594.3:c.66G>A
CA391933880
NM_152594.3:c.66G>C
CA391933883
NM_152594.3:c.66G>T